CAS No.90-04-0,o-Anisidine Suppliers

Dayang Chem (Hangzhou) Co.,Ltd.

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Simagchem Corporation

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High quality 2-Aminoanisole supplier in China

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Henan Allgreen Chemical Co.,Ltd

high quality Appearance:White or off-white Solid Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai

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Ality Chemical Corporation

The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi

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

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Hebei yanxi chemical co.,LTD.

chengdu and import and export trade co., LTD., who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do res

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Chemwill Asia Co., Ltd.

CHemwill -- o-Anisidine

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Henan Tianfu Chemical Co., Ltd.

Our company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O

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Henan Sinotech Import&Export Corporation

Chemical Name: O-Anisidine Synonyms: 2-Aminoanisole; Ortho-Anisidine; 2-methoxyaniline; 2-(o-tolyloxy)-anilin CAS No.: 90-04-0 Molecular Formula: C7H9NO Properties: colorless oily substance, melting point 6.6℃. Oxidation and discoloration i

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Henan Wentao Chemical Product Co., Ltd.

We are leading fine chemicals supplier in China and Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED intermediat

o-Anisidine 90-04-0CAS NO.: 90-04-0

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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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Hangzhou Keyingchem Co.,Ltd

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Lonwin Chemical Group Limited

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Hangzhou J&H Chemical Co., Ltd.

J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia

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Zibo Hangyu Biotechnology Development Co., Ltd

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High quality 2-Aminoanisole

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Zibo Dorne chemical technology co. LTD

Product Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,

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Siwei Development Group Ltd.

Product name: O-Anisidine CAS No.：90-04-0 Molecule Formula：C7H9NO Molecule Weight：123.15 Purity: 99.0% Package: 200kg/drum Description：Yellow oily liquid Manufacture Standards：Enterprise Standard TESTING ITEMS

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SAGECHEM LIMITED

SAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in custom synthe

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Chemsigma International Co.,Ltd.

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Kono Chem Co.,Ltd

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Hangzhou Dingyan Chem Co., Ltd

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Wuhan Fortuna Chemical Co.,Ltd

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Hunan chemfish Pharmaceutical co.,Ltd

Hunan chemfish Pharmaceutical co.,Ltd a comprehensive enterprise, is located in High-Tech Science Park,Changsha,Chia . Specializing in R&D, manufacture and marketing, we provide a wide range of products and the most professional services to meet the

Methyl 3-([(benzyloxy)carbonyl]amino)propanoate

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Aecochem Corp.

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Zhuozhou Wenxi import and Export Co., Ltd

Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard

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Antimex Chemical Limied

Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali

Benzenamine,2-methoxy-

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Xiamen AmoyChem Co.,Ltd

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Hangzhou Ocean Chemical Co., Ltd.

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Changchun Artel lmport and Export trade company

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90-04-0

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Hangzhou ZeErRui Chemical Co., Ltd.

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Synthetic route

: 578-57-4
2-bromoanisole

: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With bis(tri-ortho-tolylphosphine)palladium(0); (R)-(-)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl-di-tert-butylphosphine; ammonia; sodium t-butanolate In 1,4-dioxane at 100℃; for 12h; Inert atmosphere;	95%
With ammonium hydroxide In water at 20℃; for 9h; Green chemistry;	94%
With [N,N'-bis(5-sulfonatosalicylidene)-1,2-diaminoethane]copper disodium salt; ammonia; sodium hydroxide In water at 120℃; for 12h; sealed tube;	90%

: 91-23-6
2-Nitroanisole

: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With borane-ammonia complex In methanol; water at 20℃; for 0.0833333h;	99%
With hydrogen In neat (no solvent) at 59.84℃; under 30003 Torr; for 3.5h; Autoclave;	99.1%
With sodium tetrahydroborate In methanol; water at 20℃; for 0.0833333h; Sealed tube; Green chemistry;	99%

: 529-28-2
4-iodoanisol

: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With ammonium hydroxide In water at 20℃; for 9h; Green chemistry;	95%
With ammonium hydroxide; caesium carbonate In acetonitrile for 7h; Reflux; Green chemistry;	91%
With iron(III) oxide; sodium hydroxide; copper(l) iodide; ammonia In ethanol; water at 90℃; for 16h;	90%

: 766-51-8
2-Chloroanisole

: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With tris(dibenzylideneacetone)dipalladium (0); lithium hexamethyldisilazane; CyJohnPhos; 1,1,1-triphenylsilylamine In toluene at 100℃; for 17h;	98%
With bis(tri-ortho-tolylphosphine)palladium(0); (R)-(-)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl-di-tert-butylphosphine; ammonia; sodium t-butanolate In 1,4-dioxane at 100℃; for 24h; Inert atmosphere;	89%
With bis[chloro(1,2,3-trihapto-allylbenzene)palladium(II)]; N-[2-(di(1-adamantyl)phosphino)phenyl]morpholine; ammonia; sodium t-butanolate In 1,4-dioxane at 20℃; for 14h; Inert atmosphere; chemoselective reaction;	88%

: 20442-97-1
2-methoxylphenyl azide

: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With zinc(II) tetrahydroborate In 1,2-dimethoxyethane for 3h; Ambient temperature;	89%
Stage #1: 2-methoxylphenyl azide With hydrazine hydrate for 0.166667h; Inert atmosphere; Stage #2: for 12h; Irradiation; chemoselective reaction;	87%
With water for 5h; Inert atmosphere; UV-irradiation; Sealed tube; chemoselective reaction;	66%

: 766-51-8
2-Chloroanisole

A: 7287-75-4
N,N-bis(2-methoxyphenyl)amine

B: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With ((+/-)-binap)Ni[P(OPh)3]2*2PhCH3; ammonia; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate In 1,4-dioxane at 120℃; for 18h; Inert atmosphere; Sealed tube;	A n/a B 70%
With C28H30Cl5N3Pd; ammonia; lithium isopropoxide; sodium t-butanolate In 1,4-dioxane at 100℃; for 2h; Reagent/catalyst; Inert atmosphere; Schlenk technique;	A n/a B 68%

: 13513-82-1
1-(2-methoxyphenyl)ethanol

: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With sodium azide; trifluoroacetic acid In hexane at 40℃; for 4h; Sealed tube;	60%
With sodium azide; methanesulfonic acid; trifluoroacetic acid In hexane at 40℃; for 10h;	60%

: 91-23-6
2-Nitroanisole

A: 4342-43-2
2-methoxycyclohexanamine

B: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With hydrogen In ethanol at 100℃; under 22502.3 Torr; for 10h; Autoclave;

: 100-66-3
methoxybenzene

A: 90-04-0
2-methoxy-phenylamine

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

Conditions

Conditions	Yield
With bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]}; tert-butyl N-tosyloxycarbamate at 20℃; for 12h; chemoselective reaction;	A 37% B 37%
With titanium; sulfuric acid; hydroxylamine In water; acetonitrile at 40℃; Electrochemical reaction;
With sulfuric acid; titanium(IV); hydroxylamine; acetic acid In water at 40℃; Electrochemical reaction; Inert atmosphere;

: 91-23-6
2-Nitroanisole

: 67-63-0
isopropyl alcohol

A: C10H21NO

B: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With hydrogen In water at 130℃; under 3750.38 Torr; for 10h; Molecular sieve; Autoclave;

...Expand

: C23H32NO3PolSi

: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With trifluoroacetic acid In dichloromethane at 20℃; for 16h; Polystyrene;	52%

: 95-55-6
2-amino-phenol

: 616-38-6
carbonic acid dimethyl ester

: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With tetrabutylammomium bromide at 105℃; for 0.283333h; Reagent/catalyst; Temperature;	93%

: 3032-81-3
3,5-dichloroiodobenzene

: 5-[(2-methoxyphenyl)amino]pyrrolidin-2-one

A: 1-(3,5-dichlorophenyl)-5-[(2-methoxyphenyl)amino]pyrrolidin-2-one

B: 90-04-0
2-methoxy-phenylamine

C: 613-55-8, 18978-15-9, 19129-74-9
2,2'-dimethoxyazobenzene

Conditions

Conditions	Yield
With copper(l) iodide; caesium carbonate; N,N`-dimethylethylenediamine In 1,4-dioxane at 60℃; for 14h; Goldberg Reaction; Inert atmosphere;	A 25% B 30% C 26%

...Expand

: C20H23NO4

A: 90-04-0
2-methoxy-phenylamine

B: 582-24-1
1-phenyl-2-hydroxyethanone

Conditions

Conditions	Yield
With formic acid; 10-mesityl-10H-phenothiazine; ascorbic acid In water; acetonitrile at 20℃; for 4h; Inert atmosphere; Irradiation; Sealed tube;	A 76% B 51%

: 613-55-8, 18978-15-9, 19129-74-9
2,2'-dimethoxyazobenzene

: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With ammonium bromide; aluminium In methanol for 0.25h; sonication;	90%
With 4,4'-di-tert-butylbiphenyl; lithium; nickel dichloride In tetrahydrofuran at 20℃; Reduction;	74%
With SO2 In hydrogenchloride in the presence of I2, HI, or KI;

: 23896-88-0
formic acid o-anisidide

: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With water; sodium hydroxide In ethanol at 65 - 70℃; for 1h;	96%
With sodium hydroxide In ethanol; water at 40℃; Kinetics;

: C22H19NO4

A: 90-04-0
2-methoxy-phenylamine

B: 582-24-1
1-phenyl-2-hydroxyethanone

Conditions

Conditions	Yield
With formic acid; 10-mesityl-10H-phenothiazine; ascorbic acid In water; acetonitrile at 20℃; for 4h; Inert atmosphere; Irradiation; Sealed tube;	A 70% B 73%

: 64-18-6
formic acid

: 91-23-6
2-Nitroanisole

A: 23896-88-0
formic acid o-anisidide

B: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
platinum on charcoal; sulfided; vanadia In water at 90 - 95℃; for 2.5h;	A 24.8% B 62.8%

...Expand

: 110-71-4
1,2-dimethoxyethane

: 74-87-3
methylene chloride

: 95-55-6
2-amino-phenol

: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With sodium methylate In methanol	67.8%

...Expand

: 5720-06-9
2-Methoxyphenylboronic acid

: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With N-Bromosuccinimide; CYANAMID; bis-[(trifluoroacetoxy)iodo]benzene In acetonitrile at 20℃; for 1h; chemoselective reaction;	88%
With sodium hydroxide; hydroxylamine-O-sulfonic acid In acetonitrile at 20℃; for 16h;	80%
With N-Bromosuccinimide; N-methoxylamine hydrochloride; bis-[(trifluoroacetoxy)iodo]benzene In acetonitrile at 20℃;	79%

: 7429-44-9
2-methoxycyclohexanone

: 90-04-0
2-methoxy-phenylamine

Conditions

Conditions	Yield
With ethene; 5%-palladium/activated carbon; ammonium acetate; potassium carbonate In acetonitrile at 90℃; under 760.051 Torr; for 15h; Reagent/catalyst; Schlenk technique;	84%
With styrene; ammonium hydroxide In 1-methyl-pyrrolidin-2-one at 130℃; for 20h; Sealed tube; Inert atmosphere;	72%

: 108-24-7
acetic anhydride

: 90-04-0
2-methoxy-phenylamine

: 93-26-5
2-methoxyacetanilide

Conditions

Conditions	Yield
In dichloromethane at 20℃; Inert atmosphere;	100%
With cadmium(II) oxide at 80℃; for 0.166667h; Neat (no solvent); Microwave irradiation;	98%
With tris(pentafluorophenyl)borate In neat (no solvent) at 20℃; for 0.0166667h; Green chemistry;	95%

: 90-04-0
2-methoxy-phenylamine

: 75-36-5
acetyl chloride

: 93-26-5
2-methoxyacetanilide

Conditions

Conditions	Yield
With triethylamine In dichloromethane for 2h;	100%
With hydroxyapatite supported copper(I) oxide In acetonitrile at 50℃; for 0.0833333h;	91%
With triethylamine at 0 - 20℃; for 3h;	90%

: 90-04-0
2-methoxy-phenylamine

: 98-09-9
benzenesulfonyl chloride

: 21226-32-4
N-(2-methoxyphenyl)benzenesulfonamide

Conditions

Conditions	Yield
With pyridine for 12h; Ambient temperature;	100%
With sodium hydroxide at 20℃; for 1h; Addition;	85%
	51%

: 90-04-0
2-methoxy-phenylamine

: 107-07-3
2-chloro-ethanol

: 28005-76-7
2-[2-hydroxyethyl-(2-methoxyphenyl)amino]ethanol

Conditions

Conditions	Yield
With calcium carbonate In water at 110℃; for 72h;	100%
With potassium carbonate at 95℃; for 22h;	98%
With potassium carbonate	88%

: 90-04-0
2-methoxy-phenylamine

: 87-13-8
diethyl 2-ethoxymethylenemalonate

: 104007-09-2
2-[(2-methoxyphenylamino)-methylene]-malonic acid diethyl ester

Conditions

Conditions	Yield
In ethanol at 90℃; for 18h;	100%
at 130℃;	99%
In neat (no solvent) at 120℃; for 0.75h;	98%

: 90-04-0
2-methoxy-phenylamine

: 91-23-6
2-Nitroanisole

Conditions

Conditions	Yield
With Oxone; potassium hydroxide; disodium hydrogenphosphate; tetra(n-butyl)ammonium hydrogensulfate In dichloromethane; water; acetone at 0℃; for 0.75h; pH=7.5-8.5;	100%
With tert.-butylhydroperoxide; 3 A molecular sieve; zirconium(IV) tert-butoxide In dichloromethane for 2h; Ambient temperature;	85%
With dihydrogen peroxide; acetonitrile In aq. buffer at 20℃; for 1h; pH=11; Green chemistry;	84%

: 90-04-0
2-methoxy-phenylamine

: 407-25-0
trifluoroacetic anhydride

: 14815-12-4
N-(2-methoxyphenyl)-2,2,2-trifluoro-acetamide

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran at 0 - 20℃; for 0.75h;	100%
With pyridine In dichloromethane at 0 - 20℃; for 72h; Inert atmosphere;	99%
In diethyl ether
Stage #1: 2-methoxy-phenylamine With pyridine In dichloromethane at 0℃; for 0.5h; Stage #2: trifluoroacetic anhydride In dichloromethane at 0 - 30℃; for 1.25h;
With pyridine In dichloromethane at 0 - 20℃; for 1.25h;

: 90-04-0
2-methoxy-phenylamine

: 20442-97-1
2-methoxylphenyl azide

Conditions

Conditions	Yield
With tert.-butylnitrite; trimethylsilylazide In acetonitrile at 20℃; for 1h; Inert atmosphere;	100%
Stage #1: 2-methoxy-phenylamine With sulfuric acid; sodium nitrite In water; acetic acid at 0 - 5℃; for 0.166667h; Stage #2: With sodium azide In water; acetic acid at 0 - 5℃; for 3h;	99%
Stage #1: 2-methoxy-phenylamine With hydrogenchloride; sodium nitrite In water at 0℃; Inert atmosphere; Stage #2: With sodium azide; sodium carbonate In water at 0 - 20℃; pH=7 -Ca. 8; Inert atmosphere;	96.9%

: 5271-67-0
2-Thiophenecarbonyl chloride

: 90-04-0
2-methoxy-phenylamine

: 136340-86-8
N-(2-methoxyphenyl)-2-thiophenecarboxamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃;	100%
In toluene

: 3282-30-2
pivaloyl chloride

: 90-04-0
2-methoxy-phenylamine

: 33768-49-9
N-(2-methoxyphenyl)pivalamide

Conditions

Conditions	Yield
With sodium hydrogencarbonate In water; ethyl acetate at 20℃; for 6h;	100%
With sodium carbonate In dichloromethane Ambient temperature;	98%
With triethylamine In diethyl ether for 16h; Ambient temperature;	98%

: 74087-85-7
3,3-dimethyldioxirane

: 90-04-0
2-methoxy-phenylamine

: 91-23-6
2-Nitroanisole

Conditions

Conditions	Yield
With potassium hydroxide; disodium hydrogenphosphate; tetra(n-butyl)ammonium hydrogensulfate In dichloromethane; acetone other substituted anilines;	100%

: 90-04-0
2-methoxy-phenylamine

: 120-14-9
3,4-dimethoxy-benzaldehyde

: 82363-28-8
N-m,p-dimethoxybenzylidene-o-anisidine

Conditions

Conditions	Yield
In toluene Heating;	100%
In neat (no solvent) Time; Irradiation; Green chemistry;	72.6%
With 5A molecular sieve In toluene for 4h;

: 90-04-0
2-methoxy-phenylamine

: 623-47-2
propynoic acid ethyl ester

: 115607-78-8
ethyl 3-<(2-methoxyphenyl)amino>acrylate

Conditions

Conditions	Yield
In ethanol for 3h; Heating;	100%

: 59565-09-2
2-(vinyloxy)ethyl isothiocyanate

: 90-04-0
2-methoxy-phenylamine

: 1-(2-Methoxy-phenyl)-3-(2-vinyloxy-ethyl)-thiourea

Conditions

Conditions	Yield
at 38℃;	100%

: 90-04-0
2-methoxy-phenylamine

: 4,5,6,7-Tetrahydro-1H-benzoimidazole-5-carbonyl chloride; compound with sulfuric acid

: 131019-88-0
N-(2-methoxyphenyl)-4,5,6,7-tetrahydro-1H-benzimidazole-5-carboxamide

Conditions

Conditions	Yield
In 1,2-dichloro-ethane for 2h; Ambient temperature;	100%
In 1,2-dichloro-ethane for 2h; Ambient temperature; Yield given;

: 24424-99-5
di-tert-butyl dicarbonate

: 90-04-0
2-methoxy-phenylamine

: 154150-18-2
tert-butyl 2-methoxyphenylcarbamate

Conditions

Conditions	Yield
In tetrahydrofuran Heating;	100%
In tetrahydrofuran Inert atmosphere; Reflux;	100%
In tetrahydrofuran for 17h; Ambient temperature;	99%

: 286-20-4
cyclohexane-1,2-epoxide

: 90-04-0
2-methoxy-phenylamine

: 1-trans-2-(2-methoxyphenylamino)cyclohexanol

Conditions

Conditions	Yield
With zirconium(IV) chloride at 20℃; for 0.25h;	100%
With niobium pentachloride In dichloromethane at 20℃; for 3h;	91%
cadmium(II) chloride In dichloromethane at 20℃; for 3h;	91%

: 90-04-0
2-methoxy-phenylamine

: trifluoromethyl dihydro-1,4-dioxin-3-carbonyl chloride

: 5,6-dihydro-N-(2-methoxy)phenyl-2-trifluoromethyl-1,4-dioxin-3-carboxamide

Conditions

Conditions	Yield
Stage #1: trifluoromethyl dihydro-1,4-dioxin-3-carbonyl chloride With pyridine; polystyrene-bound 4-hydroxy-3-nitrobenzophenone In dichloromethane at 20℃; for 24h; Acylation; Stage #2: 2-methoxy-phenylamine With triethylamine In acetonitrile for 2.5h; Acylation; Heating;	100%

: 98-01-1
furfural

: 90-04-0
2-methoxy-phenylamine

: 14744-30-0
N-[(furan-2-yl)methylene]-2-methoxybenzenamine

Conditions

Conditions	Yield
In methanol at 20℃; for 24h;	100%
In water at 20℃; for 2h;	58%
In dichloromethane for 0.5h;

: 32315-10-9
bis(trichloromethyl) carbonate

: 90-04-0
2-methoxy-phenylamine

: 700-87-8
1-Isocyanato-2-methoxy-benzene

Conditions

Conditions	Yield
With triethylamine In dichloromethane	100%
In dichloromethane at 20℃; for 1.5h;
In dichloromethane at 0℃; for 0.5h;
With triethylamine In 1,2-dichloro-ethane at 0 - 85℃; for 8.5h; Inert atmosphere;
With triethylamine In 1,2-dichloro-ethane at 0 - 85℃; for 8.5h; Inert atmosphere;

: 90-04-0
2-methoxy-phenylamine

: 324541-89-1
OCHC6H3(OH)CH2C(CH2)CH2C6H3(OH)CHO

: C32H30N2O4

Conditions

Conditions	Yield
In methanol	100%

: 591-50-4
iodobenzene

: 90-04-0
2-methoxy-phenylamine

: 1207-92-7
2-methoxy-N-phenylaniline

Conditions

Conditions	Yield
With 1,1'-bis(diphenylphosphino)ferrocene; tris(dibenzylideneacetone)dipalladium (0); sodium t-butanolate In toluene at 110℃; for 12h;	100%
With palladium diacetate; sodium t-butanolate; tri tert-butylphosphoniumtetrafluoroborate In toluene at 100℃; for 24h; Schlenk technique; Inert atmosphere;	100%
With potassium hydroxide; copper(II) oxide In dimethyl sulfoxide at 110℃; for 1.7h;	98%

: 96-09-3
styrene oxide

: 90-04-0
2-methoxy-phenylamine

: 2-((2-methoxyphenyl)amino)-2-phenylethan-1-ol

Conditions

Conditions	Yield
With zirconium(IV) chloride at 20℃; for 0.25h;	100%
With activated-[Zr6O4(OH)4(BDC-C5H4NOS)6]4.5H2O3.5DMF In neat (no solvent) at 20℃; for 12h; regioselective reaction;	95%
With niobium pentachloride In dichloromethane at 20℃; for 1.5h;	91%
With tungstophosphoric acid In dichloromethane at 20℃; for 3h;	85%
With zirconyl triflate In acetonitrile at 20℃; for 1h; regioselective reaction;	82%