CAS No.104-94-9,p-Anisidine Suppliers

Dayang Chem (Hangzhou) Co.,Ltd.

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Simagchem Corporation

Welcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our

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Henan Allgreen Chemical Co.,Ltd

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Ality Chemical Corporation

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Beijing Greenchem Technology Co.,Ltd. ( Panjin Greenchem Technology Co.Ltd .)

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Chemwill Asia Co., Ltd.

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Henan Tianfu Chemical Co., Ltd.

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Henan Sinotech Import&Export Corporation

Chemical Name: P-Anisidine Synonyms: P-Aminoanisole; 4-Aminoanisole; 4-Methoxybenzeneamine; Para-Anisidine; CAS No.: 104-94-9 Molecular Formula: C7H9NO Properties: white casting flaky crystal, easily soluble in ether, ethanol, slightly solu

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Baoji Guokang Healthchem co.,ltd

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Changchun Artel lmport and Export trade company

Product Detail Minimum Order Qty. 10 Gram

p-Anisidine CAS NO.104-94-9

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Triumph International Development Limilted

Appearance:white or light yellow crystalline powder Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for research and industrial manufacture. Transportation:By

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Lonwin Chemical Group Limited

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Hangzhou Keyingchem Co.,Ltd

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Hangzhou J&H Chemical Co., Ltd.

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Chemsigma International Co.,Ltd.

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Zibo Hangyu Biotechnology Development Co., Ltd

Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi

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HANGZHOU YUNUO CHEMICAL CO.,LTD

Superior quality, moderate price & quick delivery. Appearance:white or light yellow flakes Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:Used as Pharmaceutical

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Zibo Dorne chemical technology co. LTD

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Siwei Development Group Ltd.

Product name: P-Anisidine CAS No.：104-94-9 Molecule Formula：C7H9NO Molecule Weight：123.15 Purity: 99.0% Package: 25kg/drum Description：White or yellow crystalline powder Manufacture Standards：Enterprise Standard TE

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Henan Wentao Chemical Product Co., Ltd.

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Hangzhou Zhongqi chem Co.,Ltd.

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Kono Chem Co.,Ltd

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GIHI CHEMICALS CO.,LIMITED

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Wuhan Fortuna Chemical Co.,Ltd

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Aecochem Corp.

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Zhuozhou Wenxi import and Export Co., Ltd

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Antimex Chemical Limied

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Hunan Russell Chemicals Technology Co.,Ltd

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Xiamen AmoyChem Co.,Ltd

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Synthetic route

: 100-17-4
para-methoxynitrobenzene

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With carbon monoxide; water; [Ru(cyclo-octa-1,5-diene)(pyridine)4][BPh4]2 In tetrahydrofuran at 170℃; for 20h;	100%
With hydrogen In ethyl acetate at 20℃; under 7600.51 Torr; for 4h; chemoselective reaction;	100%
With hydrogen In methanol at 20℃; for 2h;	100%

: 51-66-1
4-methoxyacetanilide

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With ammonium bromide; ethylenediamine at 70℃; for 5h; Microwave irradiation;	100%
With ammonium bromide; ethylenediamine at 70℃; for 5h; Microwave irradiation; Inert atmosphere; neat (no solvent);	99%
Stage #1: 4-methoxyacetanilide With Schwartz's reagent In tetrahydrofuran at 20℃; for 0.0333333h; Inert atmosphere; Stage #2: With water In tetrahydrofuran Inert atmosphere; chemoselective reaction;	88%

: 104-92-7
1-bromo-4-methoxy-benzene

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With ammonium hydroxide; copper(l) iodide; N,N-dimethylethylenediamine In dimethyl sulfoxide at 130℃; for 24h; Reagent/catalyst; Sealed tube; Inert atmosphere;	99%
With copper(l) iodide; 2-carboxyquinoline N-oxide; potassium carbonate; ammonium hydroxide In dimethyl sulfoxide at 80℃; for 23h; Inert atmosphere;	97%
With ammonium hydroxide In water at 20℃; for 9h; Solvent; Reagent/catalyst; Temperature; Green chemistry;	96%

: 2101-87-3
p-methoxy-phenylazide

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With iron(III) oxide; hydrazine hydrate In water at 120℃; for 1.5h; Inert atmosphere;	99%
With iron(III)-acetylacetonate; hydrazine hydrate In methanol at 150℃; for 0.0833333h; Microwave irradiation; chemoselective reaction;	98%
With hydrogen; MCM-silylamine Pd(II) In methanol at 20℃; for 1.5h; Reduction;	97%

: 52537-88-9
N-(2-hydroxybenzyl)-p-anisidine

A: 104-94-9
4-methoxy-aniline

B: C21H18O3

Conditions

Conditions	Yield
at 230℃; under 10 Torr; for 0.0833333h; Product distribution; pyrolysis without solvent, isolated as hydrochloride;	A 99% B n/a

: 92851-13-3
benzyl 4-(methoxy)phenylcarbamate

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With palladium 10% on activated carbon; silica gel; cyclohexene In methanol at 120℃; for 0.333333h; Flow reactor;	99%
With methanol; sodium tetrahydroborate; nickel(II) chloride hexahydrate at 20℃; for 0.25h; chemoselective reaction;	88%
With boron trifluoride diethyl etherate; ethanethiol for 32h; Ambient temperature;	81%
With ammonium formate; palladium on activated charcoal In isopropyl alcohol for 0.05h; Irradiation;

: 18437-68-8
tert-butyl N-(4-methoxyphenyl)carbamate

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With water at 100℃; for 6h; Inert atmosphere;	99%
In 2,2,2-trifluoroethanol at 150℃; for 2h; microwave irradiation;	98%
With kaolin In dichloromethane for 1.5h; deacylation; Heating;	97%

: 10507-69-4
4-methoxybenzohydroxamic acid

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With potassium carbonate In dimethyl sulfoxide at 90℃; for 2h; Lossen rearrangement;	99%
With potassium carbonate In dimethyl sulfoxide at 90℃; for 2h; Lossen Rearrangement;	99%
Stage #1: 4-methoxybenzohydroxamic acid With acetic anhydride; potassium carbonate In dimethyl sulfoxide at 50℃; for 2h; Lossen Rearrangement; Stage #2: With hydrogenchloride In water; dimethyl sulfoxide at 0℃;	5%
With sodium hydroxide In dimethyl sulfoxide at 80℃; for 1.5h; Lossen rearrangement;

: 83507-70-4
diethyl 2-(((4-methoxyphenyl)amino)methylene)malonate

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With ethylenediamine In ethanol at 20℃; for 0.333333h;	99%

: 623-12-1
4-chloromethoxybenzene

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With ammonium hydroxide; potassium phosphate In dimethyl sulfoxide at 80℃; UV-irradiation;	98%
With tris(dibenzylideneacetone)dipalladium (0); lithium hexamethyldisilazane; CyJohnPhos In tetrahydrofuran at 65℃; for 15h;	95%
With copper(ll) sulfate pentahydrate; ammonium hydroxide In PEG1000-DIL; methyl cyclohexane at 60℃; for 8h;	90%

: 92097-26-2
(4-Methoxy-phenyl)-carbamic acid (E)-4-trimethylsilanyl-but-2-enyl ester

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With methanol; tetrakis(triphenylphosphine) palladium(0) In dichloromethane for 0.333333h; Ambient temperature;	97%

: 696-62-8
para-iodoanisole

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With ammonium hydroxide; copper(l) iodide; N,N-dimethylethylenediamine In dimethyl sulfoxide at 130℃; for 18h; Reagent/catalyst; Time; Sealed tube; Inert atmosphere;	97%
With ammonium hydroxide In water at 20℃; for 9h; Green chemistry;	97%
Stage #1: para-iodoanisole With potassium phosphate; 2,2,2-trifluoroacetamide; N,N`-dimethylethylenediamine; copper(l) iodide In N,N-dimethyl-formamide at 45℃; Stage #2: With methanol In N,N-dimethyl-formamide at 45℃; Further stages.;	95%

: 965-50-4
N-(4-methoxyphenyl)-3-oxo-3-phenylpropanamide

: 95-54-5
1,2-diamino-benzene

A: 104-94-9
4-methoxy-aniline

B: 716-79-0
2-phenyl-1H-benzoimidazole

Conditions

Conditions	Yield
With 1-n-butyl-3-methylimidazolim bromide In neat (no solvent) at 120℃; for 1.5h;	A 92% B 97%

...Expand

: 1562-94-3, 21650-70-4, 51437-65-1
4,4'-dimethoxyazoxybenzene

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With N-doped TiO2 In methanol at 20℃; for 3h; UV-irradiation; Inert atmosphere;	95%
With 4,4'-di-tert-butylbiphenyl; lithium; nickel dichloride In tetrahydrofuran at 20℃; for 2h; Reduction; deoxygenation;	57%

: 5437-98-9
4'-methoxyacetoacetanilide

: 95-54-5
1,2-diamino-benzene

A: 615-15-6
2-Methyl-1H-benzimidazole

B: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With 1-n-butyl-3-methylimidazolim bromide In neat (no solvent) at 120℃; for 1h;	A 95% B 93%

...Expand

: 696-62-8
para-iodoanisole

: 639-58-7
triphenyltin chloride

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With bis[(2-methylacetatobenzyl)tri(p-tolyl)phosphonium] hexabromodipalladate(II); potassium carbonate at 90℃; for 0.3h; Stille Cross Coupling; Green chemistry;	95%

: 1227-44-7
N,N'-bis(4-methoxyphenyl)urea

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With 3-azapentane-1,5-diamine at 130℃; for 12h; Sealed tube;	94%
In water at 150℃; Green chemistry;

: 1227-45-8
1,3-bis-(p-methoxyphenyl)thiourea

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With ammonium bromide; ethylenediamine at 80℃; for 5h; Microwave irradiation;	94%
With 3-azapentane-1,5-diamine at 130℃; for 12h; Sealed tube;	92%

: 501-58-6
bis(4-methoxyphenyl)diazene

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With aminomethyl polysterene resine formic acid salt; zinc In methanol at 20℃; for 0.333333h;	93%
With potassium hydroxide; nickel-incorporated hexagonal mesoporous aluminophosphate In isopropyl alcohol at 82.84℃; for 1.5h;	91%
With zinc In methanol at 25℃; for 0.216667h; Inert atmosphere;	90%

: 78-83-1
2-methyl-propan-1-ol

: 458-52-6
2-fluoro-4-(methoxy)aniline

A: 71182-60-0
N-isobutyl-N-(4-methoxyphenyl)amine

B: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With methanesulfonato(2-dicyclohexylphosphino -2’,6’-di-i-propoxy-1,1‘-biphenyl)(2’-amino-1,1’-biphenyl-2-yl)palladium(II); sodium tert-pentoxide In toluene at 80℃; for 72h; Sealed tube; Inert atmosphere;	A 93% B 2%

...Expand

: 1227-44-7
N,N'-bis(4-methoxyphenyl)urea

A: 67-56-1
methanol

B: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With C25H19BrMnN2O2P; potassium tert-butylate; hydrogen In toluene at 130℃; under 15001.5 Torr; for 48h;	A 90 %Spectr. B 93%

: 635-46-1
1,2,3,4-tetrahydroisoquinoline

: 100-17-4
para-methoxynitrobenzene

A: 91-22-5
quinoline

B: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With nickel-nitrogen-doped carbon framework In water at 145℃; for 18h; Inert atmosphere; Sealed tube; Green chemistry;	A 92% B 93%

...Expand

: 58960-03-5
7-methyl-1,2,3,4-tetrahydroquinoline

: 100-17-4
para-methoxynitrobenzene

A: 612-60-2
7-methylquinoline

B: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With nickel-nitrogen-doped carbon framework In water at 145℃; for 18h; Inert atmosphere; Sealed tube; Green chemistry;	A 92% B 92%

...Expand

: 110228-48-3
4'-methoxybiphenyl-2-sulphenanilide

A: 5051-19-4
2,7-dimethoxyphenazine

B: 19813-97-9
1-phenyl-2-[(2-phenylphenyl)disulfanyl]benzene

C: 104-94-9
4-methoxy-aniline

D: 501-58-6, 21650-55-5, 82570-64-7
(E)-1,2-bis(4-methoxyphenyl)diazene

Conditions

Conditions	Yield
In benzene at 150℃; for 40h; Further byproducts given;	A 26% B 91% C 17% D 12%
In benzene at 85℃; for 720h; Further byproducts given;	A 12% B 81% C 29% D 12%

...Expand

: 5720-07-0
4-methoxyphenylboronic acid

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With N-Bromosuccinimide; CYANAMID; bis-[(trifluoroacetoxy)iodo]benzene In acetonitrile at 20℃; for 1h; chemoselective reaction;	91%
With copper(I) oxide; ammonium hydroxide; oxygen; sodium hydroxide In water at 25℃; for 15h;	88%
With sodium hydroxide; hydroxylamine-O-sulfonic acid In acetonitrile at 20℃; for 16h;	86%

: 1336-21-6
ammonium hydroxide

: 104-92-7
1-bromo-4-methoxy-benzene

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With copper(l) iodide In water at 200℃; for 2h; Autoclave;	91%
With copper(ll) sulfate pentahydrate; potassium phosphate tribasic heptahydrate; water; Sucrose In water at 90℃; for 15h; Catalytic behavior; Reagent/catalyst; Solvent; Green chemistry;	85%

: 371779-94-1
N,N-bis(1,1-dioxo-1,2-benzisothiazol-3-yl)-4-methoxyaniline

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With sodium tetrahydroborate In tetrahydrofuran for 12h;	90%

: C19H18ClNO2

: 109-77-3
malononitrile

A: 104-94-9
4-methoxy-aniline

B: 137100-26-6
1-chloro-6-methoxy-2-[β,β-dicyano]-3,4-dihydronaphthalene

Conditions

Conditions	Yield
With sodium dodecyl-sulfate In water at 25 - 30℃; for 0.166667h;	A n/a B 90%

...Expand

: 171364-79-7
2-(4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

: 104-94-9
4-methoxy-aniline

Conditions

Conditions	Yield
With water; sodium hydroxide; hydroxylamine-O-sulfonic acid In acetonitrile at 20℃; for 16h;	90%
With O-Methylhydroxylamin; n-butyllithium In tetrahydrofuran; hexane at -78 - 60℃; for 24h; Inert atmosphere; Cooling with acetone-dry ice; stereospecific reaction;	87%

: 7472-54-0
N-(p-methoxyphenyl)benzamide

A: 104-94-9
4-methoxy-aniline

B: 100-51-6
benzyl alcohol

Conditions

Conditions	Yield
With hydrogen In toluene at 160℃; under 45004.5 Torr; for 15h; Catalytic behavior; Autoclave;	A 90% B 82%
With potassium tert-butylate; hydrogen; [Ru(PtBuNNHBn)H(CO)Cl] In tetrahydrofuran at 19 - 24℃; under 7500.75 Torr; for 68h;	A 92 %Chromat. B 92 %Chromat.

: 98-01-1
furfural

: 104-94-9
4-methoxy-aniline

: 1749-14-0, 100239-11-0
N-furfurylidene-p-anisidine

Conditions

Conditions	Yield
With sodium sulfate In benzene for 0.5h; Ambient temperature;	100%
In methanol at 20℃; for 24h;	100%
In methanol at 20℃; for 24h;	100%

: 109-09-1
2-chloropyridine

: 104-94-9
4-methoxy-aniline

: 78644-78-7
N-(4-methoxyphenyl)pyridin-2-amine

Conditions

Conditions	Yield
at 160℃; for 6h; Inert atmosphere; Neat (no solvent);	100%
With palladium 10% on activated carbon; sodium t-butanolate; CyJohnPhos In tert-Amyl alcohol at 110℃; Buchwald-Hartwig amination; Inert atmosphere;	73%
With sodium dispersion In tetrahydrofuran at 50℃; for 1h;	65.6%
With zinc(II) chloride at 220 - 230℃;

: 108-24-7
acetic anhydride

: 104-94-9
4-methoxy-aniline

: 51-66-1
4-methoxyacetanilide

Conditions

Conditions	Yield
In dichloromethane at 20℃; Inert atmosphere;	100%
With silver trifluoromethanesulfonate at 60℃; for 0.0166667h; neat (no solvent);	99%
With cadmium(II) oxide at 80℃; for 0.0833333h; Neat (no solvent); Microwave irradiation;	98%

: 104-88-1
4-chlorobenzaldehyde

: 104-94-9
4-methoxy-aniline

: 1749-03-7
N-(4-chlorobenzylidene)-4-methoxyaniline

Conditions

Conditions	Yield
for 6h; Ambient temperature;	100%
In ethanol for 1h; Sonication;	100%
at 20℃; for 14h; Molecular sieve;	99%

: 555-16-8
4-nitrobenzaldehdye

: 104-94-9
4-methoxy-aniline

: 5455-87-8
4-methoxy-N-(4-nitrobenzylidene)aniline

Conditions

Conditions	Yield
at 50℃; for 24h;	100%
for 6h; Molecular sieve; Reflux;	100%
In ethanol for 3h; Reflux;	95%

: 100-52-7
benzaldehyde

: 104-94-9
4-methoxy-aniline

: 783-08-4
[4-(benzylideneamino)phenyl]methanol

Conditions

Conditions	Yield
In toluene for 1h; Ambient temperature;	100%
In ethanol for 1h; Sonication;	100%
In dichloromethane at 20℃; Molecular sieve;	99%

: 123-08-0
4-hydroxy-benzaldehyde

: 104-94-9
4-methoxy-aniline

: 3230-50-0
N-(4-hydroxylbenzylidene)-4-methoxyaniline

Conditions

Conditions	Yield
for 6h; Ambient temperature;	100%
With sulfuric acid In neat (no solvent) Microwave irradiation; Sealed tube; Green chemistry;	93%
In ethanol for 5h; Reflux;	88%

: 123-11-5
4-methoxy-benzaldehyde

: 104-94-9
4-methoxy-aniline

: 1749-08-2
N-(4-methoxy benzylidene)-4-methoxyaniline

Conditions

Conditions	Yield
In ethanol for 1h; Sonication;	100%
With magnesium sulfate In dichloromethane at 20℃; for 72h;	99%
In ethyl 2-hydroxypropionate; water at 20℃; for 0.05h;	93%

: 75-15-0
carbon disulfide

: 104-94-9
4-methoxy-aniline

: 2284-20-0
4-Methoxyphenyl isothiocyanate

Conditions

Conditions	Yield
Stage #1: carbon disulfide; 4-methoxy-aniline With triethylamine In ethanol at 20℃; Stage #2: With dmap; di-tert-butyl dicarbonate In ethanol at 20℃; for 0.25h; Further stages.;	100%
Stage #1: carbon disulfide; 4-methoxy-aniline With triethylamine In ethanol at 20℃; for 1h; Stage #2: With dmap; di-tert-butyl dicarbonate at 0 - 20℃; for 4h;	96%
Stage #1: carbon disulfide; 4-methoxy-aniline With triethylamine In methanol at 0 - 5℃; Stage #2: With bis(trichloromethyl) carbonate In chloroform at 0℃; for 4h; Further stages.;	95%

: 64-18-6
formic acid

: 104-94-9
4-methoxy-aniline

: 5470-34-8
4-methoxyformanilide

Conditions

Conditions	Yield
In toluene Reflux;	100%
With sodium formate at 20℃; for 3h; Neat (no solvent);	99%
With TiO2-SO4(2-) In acetonitrile at 20℃; for 4h;	99%

: 104-94-9
4-methoxy-aniline

: 121-33-5
vanillin

: 24033-07-6
4-methoxy-N-(4-hydroxy-3-methoxybenzylidene)aniline

Conditions

Conditions	Yield
for 2h; Ambient temperature;	100%
In ethanol for 3h; Reflux;	99.2%
sodium hydrogen sulfate; silica gel at 60 - 62℃; for 0.0222222h; microwave irradiation;	98%

: 104-94-9
4-methoxy-aniline

: 75-03-6
ethyl iodide

: 15144-80-6
N,N-diethyl-4-methoxyaniline

Conditions

Conditions	Yield
With sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; for 15h;	100%
With sodium hydroxide at 120℃;

: 104-94-9
4-methoxy-aniline

: 556-61-6
methyl thioisocyanate

: 20333-73-7
1-(4-methoxyphenyl)-3-methyl-thiourea

Conditions

Conditions	Yield
at 20℃; for 24h; Addition; solid-phase reaction;	100%
With ethanol
In ethanol for 1h; Heating;
In ethanol Reflux;

: 104-94-9
4-methoxy-aniline

: 292638-85-8
acrylic acid methyl ester

: 42313-52-0
methyl 3-(4-methoxyphenylamino)propanoate

Conditions

Conditions	Yield
With silica-supported aluminum chloride at 60℃; for 1.5h; Michael addition; Neat (no solvent);	100%
In water at 50℃; for 24h; Michael condensation;	94%
With lithium tetrafluoroborate at 70℃; for 0.166667h; Michael condensation; Neat (no solvent);	93%

: 104-94-9
4-methoxy-aniline

: 79-04-9
chloroacetyl chloride

: 22303-36-2
N-(4-methoxyphenyl)-2-chloroacetamide

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0℃; for 0.166667h;	100%
In tetrahydrofuran at 20℃; for 18h;	100%
With triethylamine In dichloromethane at 0 - 25℃;	99.4%

: 104-94-9
4-methoxy-aniline

: 104-55-2
3-phenyl-propenal

: 15286-52-9, 22835-33-2, 80542-40-1, 88315-63-3, 101535-86-8, 123525-44-0
N-(4-Methoxyphenyl)-3-phenylpropenaldimine

Conditions

Conditions	Yield
piperidine In ethanol for 5h; Heating;	100%
With magnesium sulfate In dichloromethane at 20℃;	100%
In ethyl 2-hydroxypropionate; water at 20℃; for 0.025h;	96%

: 104-94-9
4-methoxy-aniline

: 1885-14-9
phenyl chloroformate

: 20950-96-3
(4-methoxyphenyl)carbamic acid phenyl ester

Conditions

Conditions	Yield
With pyridine In ethyl acetate at 20℃; for 1h;	100%
With sodium hydrogencarbonate In tetrahydrofuran; water at 0 - 20℃; for 0.0833333h;	97%
With sodium carbonate In tetrahydrofuran; water; ethyl acetate at 0 - 20℃;	92%

: 104-94-9
4-methoxy-aniline

: 98-59-9
p-toluenesulfonyl chloride

: 1150-26-1
N-(4-Methoxy-phenyl)-4-methyl-benzenesulfonamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 4℃;	100%
With pyridine for 16h; Reflux;	97%
With dendritic fibrous nanosilica KCC-1 3-aminopropyl-functionalized supported on Fe3O4 magnetic nanocatalyst In water at 20℃; for 0.5h; Solvent; Temperature; Reagent/catalyst; Time; Green chemistry;	97%

: 104-94-9
4-methoxy-aniline

: 97-00-7
1-chloro-2,4-dinitro-benzene

: 967-35-1
N-(4-methoxyphenyl)-2,4-dinitrobenzenamine

Conditions

Conditions	Yield
With sodium carbonate In ethanol Heating;	100%
In benzene at 40℃; Rate constant; Mechanism; other solvent;
With tetrabutyl-ammonium chloride In benzene at 30℃; Rate constant; different substrate concentrations;

: 104-94-9
4-methoxy-aniline

: 407-25-0
trifluoroacetic anhydride

: 332-34-3
2,2,2-trifluoro-N-(4-methoxy-phenyl)-acetamide

Conditions

Conditions	Yield
With sodium hydride In N,N-dimethyl-formamide at 20℃;	100%
With triethylamine In tetrahydrofuran at 0 - 20℃; for 0.75h;	100%
at 20℃; for 1h;	98.3%

: 104-94-9
4-methoxy-aniline

: 121-90-4
m-nitrobenzoic acid chloride

: 101971-72-6
N-(4'-methoxyphenyl)-3-nitrobenzamide

Conditions

Conditions	Yield
In pyridine Heating;	100%
With pyridine Reflux;	85%
With triethylamine In acetone at 20℃;	47%

: 104-94-9
4-methoxy-aniline

: 100-51-6
benzyl alcohol

: 17377-95-6
benzyl(4-methoxyphenyl)amine

Conditions

Conditions	Yield
With chloro(η5-pentamethylcyclopentadienyl)(L-prolinato)iridium(III) In toluene at 95℃; for 24h; Inert atmosphere; Sealed tube;	100%
With potassium tert-butylate; copper diacetate In 1,4-dioxane at 130℃; for 48h;	99%
With potassium tert-butylate; copper diacetate In 1,4-dioxane at 130℃; for 48h; Inert atmosphere;	99%

: 104-94-9
4-methoxy-aniline

: 87-13-8
diethyl 2-ethoxymethylenemalonate

: 83507-70-4
diethyl 2-(((4-methoxyphenyl)amino)methylene)malonate

Conditions

Conditions	Yield
at 14 - 95℃; for 2.91667h;	100%
In ethanol for 4h; Heating / reflux;	100%
at 100 - 125℃; for 18.5h;	100%

: 104-94-9
4-methoxy-aniline

: 2101-87-3
p-methoxy-phenylazide

Conditions

Conditions	Yield
With tert.-butylnitrite; trimethylsilylazide In acetonitrile at 0 - 20℃; for 1h;	100%
With 2-azido-1,3-dimethyl-4,5-dihydro-1H-imidazol-3-ium hexafluorophosphate (V); triethylamine In dichloromethane at 20℃; for 0.166667h; Solvent; Reagent/catalyst; Temperature; Inert atmosphere;	100%
Stage #1: 4-methoxy-aniline With hydrogenchloride; sodium nitrite In water for 0.5h; Cooling with ice; Stage #2: With sodium azide In water at 20℃; for 2h; Cooling with ice;	100%

: 126-81-8
dimedone

: 104-94-9
4-methoxy-aniline

: 24706-48-7
3-[(4-methoxyphenyl)amino]-5,5-dimethylcyclohex-2-en-1-one

Conditions

Conditions	Yield
at 20℃; for 0.5h; Solid phase reaction; condensation;	100%
With silica-supported phosphorous pentoxide at 80℃; for 0.05h; Neat (no solvent); chemoselective reaction;	97%
With silica sulfuric acid In acetonitrile for 0.0166667h; Microwave irradiation;	97%

: 104-94-9
4-methoxy-aniline

: 135-19-3
β-naphthol

: 13411-91-1
1-(4-methoxyphenylazo)naphthalen-2-ol

Conditions

Conditions	Yield
With potassium hydrogensulfate; water; sodium nitrite Diazotization; coupling; microwave irradiation;	100%
Stage #1: 4-methoxy-aniline With ferric hydrogen sulphate; silica gel; sodium nitrite In water Green chemistry; Stage #2: β-naphthol In water at 20℃; for 0.05h; Green chemistry; regioselective reaction;	97%
Stage #1: 4-methoxy-aniline With water; sodium nitrite In neat (no solvent) at 20℃; Stage #2: β-naphthol In neat (no solvent) at 20℃; for 0.25h;	94%

: 1121-60-4
pyridine-2-carbaldehyde

: 104-94-9
4-methoxy-aniline

: 26930-67-6, 42910-70-3
(E)-N-(4-methoxyphenyl)-1-(pyridin-2-yl)methanimine

Conditions

Conditions	Yield
In toluene at 20℃; for 24h;	100%
With magnesium sulfate In benzene for 20h; Ambient temperature;	98%
With magnesium sulfate In ethanol at 25℃; for 16h;	91%