DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
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inquiryWelcome 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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inquiryProduct description: Product name 4-Methoxybenzyl cyanide CAS number 104-47-2 Assay ≥99% Appearance Colorless to yellowish transparent liquid Capacity 200mt/year Application
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inquiryThe 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
Cangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new ap
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inquiry1. Product advantages High purity, all above 98.5%, no impurities after dissolution We will test each batch to ensure quality OEM and private brand services designed for free Various cap colors available We can also provide MT1 peptide powd
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inquiryAppearance:Clear colorless to slightly yellow liquid Storage:room temperature Package:200kg/Drum Application: 4-Methoxyphenylacetonitrile was used as starting reagent in the synthesis of : 2-(1-cyano-1-(2-methoxy)phenyl)methylidene-3-phenylthiazol
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inquiry1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; Appearance:White Crystalline Powder Storage:Store in sealed conta
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inquiry1.No Less 8 years exporting experience. Clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specialized
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inquiry4-Methoxybenzyl cyanide CAS:104-47-2 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic int
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
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inquiryProduct Name: 4-Methoxybenzyl cyanide Synonyms: 4-METHOXYBENZYL CYANIDE;(4-METHOXYPHENYL)ACETONITRILE;4-ANISYL CYANIDE;HOMOANISONITRILE;LABOTEST-BB LT00848055;P-ANISYLACETONITRILE;P-ANISYL CYANIDE;P-CYANOMETHYLANISOLE CAS: 104-47-2 MF: C9H9N
Cas:104-47-2
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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inquiry4-MethoxyphenylacetonitrilesAppearance:white powder Storage:kept in a cool, dry and ventilated place Package:according to customers' requirements Application:BPC(bulk pharmaceutical chemicals) Transportation:By air(EMS or EUB or FedEx or TNT ect...)
We are one of a few suppliers that can offer custom synthesis service of this product We are specialized in custom synthesis, chemical/pharmaceutical/ pesticides outsourcing and contract research. We are committed to prov
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inquirySuperior quality Appearance:Clear colorless to slightly yellow liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:4-Methoxyphenylacetonitrile
Product name: 4-Methoxyphenylacetonitrile CAS No.: 104-47-2 Molecule Formula:C9H9NO Molecule Weight:147.17 Purity: 98.0% Package: 200kg/drum Description:Light yellow to colorless transparent liquid Manufacture Standards:Enterprise Sta
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inquiryChemical Names: 4-Methoxyphenylacetonitrile, (4-Methoxyphenyl)acetonitrile, 4-Methoxybenzyl cyanide Chemical Structure: Molecular Formula: C9H9NO CAS:
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inquiryGMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride In benzene Heating; | A 94% B 100% |
lysichitalexin
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With dmap; Sn(thiophenolate)4; tributylphosphine; diethylazodicarboxylate In dichloromethane at 0℃; for 0.0833333h; | 99% |
Multi-step reaction with 3 steps 1: 83 percent / NaNO2, NaOH / methanol / 0 °C 2: 63 percent / Et3N / CH2Cl2 / Ambient temperature 3: 94 percent / Bu3SnH, AIBN / benzene / Heating View Scheme | |
Multi-step reaction with 2 steps 1: tris(2,2'-bipyridyl)ruthenium(II)chloride hexahydrate; N-ethyl-N,N-diisopropylamine; magnesium(II) perchlorate / acetonitrile / 12 h / 20 °C / Inert atmosphere; Irradiation 2: triphenylphosphine; iodine / dichloromethane / 8 h / 20 °C / Inert atmosphere View Scheme |
Conditions | Yield |
---|---|
at 520 - 550℃; under 0.01 Torr; | 98% |
With 1,1-Diphenylethylene In various solvent(s) at 210℃; Rate constant; Thermodynamic data; ΔG(excit.) <250 deg C>; ΔH(excit.), ΔS(excit.); | 101 % Chromat. |
With 1,1-diphenylene; chlorobenzene In benzene at 170℃; Rate constant; Thermodynamic data; also at 190, 210 and 230 deg C; ΔHY (excit.), ΔΔHY-H(excit.), ΔSY(excit.), ΔΔSY-H(excit); |
Conditions | Yield |
---|---|
With triethylamine; ethanaminium,N-(difluoro-λ4-sulfanylidene)-N-ethyl-,tetrafluoroborate In ethyl acetate at 20℃; for 1h; Inert atmosphere; | 98% |
With thionyl chloride In benzene Reflux; |
2-(4-methoxy-benzyloxy)-tetrahydro-pyran
tetra-n-butylammonium cyanide
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With triphenylphosphine; 2,3-dicyano-5,6-dichloro-p-benzoquinone In acetonitrile for 3h; Heating; | 95% |
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With TEA In dichloromethane at 25℃; for 2h; | 95% |
Conditions | Yield |
---|---|
With phosphorus tribromide In benzene for 5h; Heating; | 93% |
2-[(Z)-Hydroxyimino]-3-(4-methoxy-phenyl)-propionic acid
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With 1,1'-carbonyldiimidazole In benzene 1.) r.t., 15 min, 2.) 68-70 deg C, 1 h; | 93% |
4-methoxy-1-(methoxymethoxy)methyl benzene
tetra-n-butylammonium cyanide
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With 1-methyl-3H-imidazolium nitrate at 135 - 140℃; for 0.05h; Microwave irradiation; | 93% |
With phosphotungstic acid at 130 - 142℃; for 0.05h; Microwave irradiation; Ionic liquid; chemoselective reaction; | 88% |
With 1-(n-butyl)-3-methylimidazolium tetrachloroindate at 135 - 140℃; for 0.0916667h; Microwave irradiation; Neat (no solvent); chemoselective reaction; | 82% |
tetra-n-butylammonium cyanide
4-Methoxybenzyl alcohol
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With triphenylphosphine; 2,3-dicyano-5,6-dichloro-p-benzoquinone In acetonitrile at 20℃; | 92% |
Conditions | Yield |
---|---|
With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; bis(η3-allyl-μ-chloropalladium(II)) In 1,3,5-trimethyl-benzene at 20 - 140℃; for 5.16667h; Inert atmosphere; Sealed tube; chemoselective reaction; | 92% |
(E)-2-(4-methoxyphenyl)acetaldehyde oxime
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With iodine; triphenylphosphine In dichloromethane at 20℃; for 8h; Inert atmosphere; | 92% |
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With potassium fluoride In water; N,N-dimethyl-formamide at 125℃; for 16h; Inert atmosphere; | 91% |
Conditions | Yield |
---|---|
With 1,1'-oxalyldiimidazole In benzene 1.) r.t., 15 min, 2.) 68-70 deg C, 1 h; | 90% |
With acetic anhydride at 100℃; |
Conditions | Yield |
---|---|
With triethylamine; tetra-(n-butyl)ammonium iodide In N,N-dimethyl-formamide for 3h; Heating; | 90% |
Conditions | Yield |
---|---|
With sodium azide; TEA; triethylphosphine; (bis-(2-methoxyethyl)amino)sulfur trufluoride In dichloromethane; dimethyl sulfoxide at 0℃; for 30h; | 90% |
Conditions | Yield |
---|---|
With triethylamine; ethanaminium,N-(difluoro-λ4-sulfanylidene)-N-ethyl-,tetrafluoroborate In ethyl acetate at 20℃; for 1h; Inert atmosphere; | 90% |
With p-toluenesulfonyl chloride In acetonitrile at 0℃; for 8h; Inert atmosphere; |
Conditions | Yield |
---|---|
With TEA; trichloroisocyanuric acid In N,N-dimethyl-formamide at 15℃; for 4h; | 89% |
With iodine; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In dimethyl sulfoxide at 65℃; for 1.5h; | 58% |
With HRu(1,3-bis(6'-methyl-2'-pyridylimino)isoindoline)(PPh3)2 In toluene at 110℃; for 24h; Inert atmosphere; Glovebox; chemoselective reaction; | 48% |
With [Ru(p-cymene)(pzH-NP)(Cl)]Cl; potassium tert-butylate In toluene at 70℃; for 24h; Schlenk technique; Inert atmosphere; | 43% |
Conditions | Yield |
---|---|
With polyethylene glycol functionalized magnetic dicationic ionic liquid In water for 1h; Reflux; Green chemistry; | 88% |
In ethanol; water for 4h; Reflux; | 58% |
In acetonitrile Reflux; | |
In acetonitrile for 4h; Reflux; |
Conditions | Yield |
---|---|
Stage #1: 4-cyanomethylphenol With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.5h; Inert atmosphere; Stage #2: methyl iodide In N,N-dimethyl-formamide at 20℃; for 72h; Inert atmosphere; | 87% |
With potassium hydroxide | |
With potassium hydroxide at 100℃; |
sodium cyanide
1-(4-Methoxy-benzyl)-2-methylsulfanyl-4,6-diphenyl-pyridinium; iodide
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
In 1,2-dimethoxyethane for 24h; Heating; | 87% |
C10H12BrNO2
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With acetic acid; zinc In N,N-dimethyl-formamide at 150℃; for 0.5h; | 86% |
With sodium carbonate In methanol for 2h; Irradiation; | 80% |
4-methoxyphenylboronic acid
2-aminoacetonitrile hydrochloride
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With sodium nitrite In water; toluene at 50℃; for 24h; Schlenk technique; | 86% |
Conditions | Yield |
---|---|
In dimethyl sulfoxide | 85% |
With acetone; potassium iodide | |
In dimethyl sulfoxide at 45 - 50℃; for 5h; | |
With acetone; potassium iodide |
Conditions | Yield |
---|---|
In tetrahydrofuran at 80℃; for 11h; | 82% |
4-methoxy-1-[(ethoxymethoxy)methyl]benzene
tetra-n-butylammonium cyanide
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With 1-(n-butyl)-3-methylimidazolium tetrachloroindate at 135 - 140℃; for 0.0916667h; Microwave irradiation; Neat (no solvent); chemoselective reaction; | 82% |
Conditions | Yield |
---|---|
With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; palladium diacetate; sodium carbonate In 1,4-dioxane; water at 60℃; for 12h; Inert atmosphere; Sealed tube; | 81% |
1'p.methoxyphenyl 1'-cyano 1,3,5,5-tetramethyl 2-cyclohexen 1-ol
A
3,5,5-Trimethylcyclohex-2-en-1-one
B
p-methoxyphenyl-3' cyano-3' tetramethyl-3,3,5,5 cyclohexanone
C
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide at -70℃; for 0.0833333h; Yield given; | A n/a B 80% C n/a |
With n-butyllithium In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide at -70℃; for 0.0833333h; Yields of byproduct given; | A n/a B 80% C n/a |
Conditions | Yield |
---|---|
With iron(III) trifluoromethanesulfonate In 1,2-dichloro-ethane at 80℃; for 2h; | 78% |
1-bromo-4-methoxy-benzene
tri-n-butyl(cyanomethyl)stannane
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
dichlorobis(tri-O-tolylphosphine)palladium In m-xylene at 120℃; for 3h; | 77% |
p-methoxybenzylnitrile
carbonic acid dimethyl ester
methyl 2-cyano-2-(4-methoxyphenyl) acetate
Conditions | Yield |
---|---|
With sodium hydride In toluene; mineral oil at 80℃; for 5.5h; | 100% |
With sodium hydride In toluene at 80℃; for 5h; Inert atmosphere; Cooling with ice; | 81% |
With sodium methylate In methanol; toluene at 75 - 80℃; for 12h; | 42% |
mechlorethamine hydrochloride
p-methoxybenzylnitrile
4-(4-methoxyphenyl)-1-methylpiperidine-4-carbonitrile
Conditions | Yield |
---|---|
With sodium hydride In DMF (N,N-dimethyl-formamide) at 0 - 60℃; for 24h; | 100% |
With tetra(n-butyl)ammonium hydrogensulfate In sodium hydroxide | 20% |
p-methoxybenzylnitrile
3-oxa-1,5-dichloropentane
4-(4-methoxyphenyl)tetrahydro-2H-pyran-4-carbonitrile
Conditions | Yield |
---|---|
Stage #1: p-methoxybenzylnitrile With sodium hydride In DMF (N,N-dimethyl-formamide) at 0 - 20℃; for 0.5h; Stage #2: 3-oxa-1,5-dichloropentane In DMF (N,N-dimethyl-formamide) at 0 - 20℃; for 2.33333h; | 100% |
Stage #1: p-methoxybenzylnitrile With sodium hydroxide In N,N-dimethyl-formamide for 0.5h; Stage #2: 3-oxa-1,5-dichloropentane In N,N-dimethyl-formamide at 80 - 100℃; for 5h; | 69% |
With sodium hydride In N,N-dimethyl-formamide; mineral oil Cooling with ice; | 64% |
With NaH In dimethyl sulfoxide |
(Z)-N-benzylidenebenzylamine N-oxide
Triethylsilyl trifluoromethanesulfonate
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With triethylamine In 1,2-dichloro-ethane at -30℃; for 0.5h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With hydrogenchloride; hydrogen In propan-1-ol; water at 60℃; under 375.038 Torr; for 18h; Flow reactor; | 100% |
Stage #1: p-methoxybenzylnitrile With MnBr(CO)2[NH(CH2CH2P(iPr)2)2]; hydrogen; sodium t-butanolate In toluene at 120℃; under 37503.8 Torr; for 36h; Autoclave; Stage #2: With hydrogenchloride In diethyl ether | 96% |
Stage #1: p-methoxybenzylnitrile With borane-ammonia complex; C17H16BrMnN2O3S In hexane at 60℃; for 6h; Stage #2: With hydrogenchloride In diethyl ether; water | 96% |
Stage #1: p-methoxybenzylnitrile With ammonium hydroxide; hydrogen In water; isopropyl alcohol at 130℃; under 30003 Torr; for 2h; Autoclave; Stage #2: With hydrogenchloride In methanol | 85% |
Multi-step reaction with 2 steps 1: hydrogen; ammonium hydroxide / isopropyl alcohol / 15 h / 120 °C / 22502.3 Torr / Autoclave 2: hydrogenchloride / methanol View Scheme |
p-methoxybenzylnitrile
1-Phenylbut-1-en-3-one
(methoxy-4 phenyl)-1 phenyl-2 oxo-4 pentane carbonitrile
Conditions | Yield |
---|---|
With sodium methylate In methanol for 4h; Ambient temperature; | 99% |
With tetrabutylammomium bromide; potassium carbonate In toluene at 50℃; for 6h; | 70% |
p-methoxybenzylnitrile
4-Bromo-5,6-dimethyl-furo[2,3-d]pyrimidine
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide at 130℃; for 0.5h; | 99% |
Conditions | Yield |
---|---|
With lithium diisopropyl amide In tetrahydrofuran at -10 - 20℃; Condensation; cyclization; | 99% |
{1-[chloro(p-tolylsulfinyl)methyl]cyclobutyl}acetonitrile
p-methoxybenzylnitrile
6-amino-7-(4-methoxyphenyl)spiro[3.4]octa-5,7-diene-5-carbonitrile
Conditions | Yield |
---|---|
Stage #1: {1-[chloro(p-tolylsulfinyl)methyl]cyclobutyl}acetonitrile With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 0.5h; Stage #2: p-methoxybenzylnitrile With n-butyllithium In tetrahydrofuran at -78 - -40℃; for 1.5h; Further stages.; | 99% |
C-phenyl-N-methylnitrone
Triethylsilyl trifluoromethanesulfonate
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With triethylamine In 1,2-dichloro-ethane at -30℃; for 0.5h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With sodium methylate In methanol; ethanol at 20℃; for 0.166667h; | 99% |
With sodium ethanolate In ethanol at 40℃; for 0.666667h; Knoevenagel Condensation; | 91% |
p-methoxybenzylnitrile
isopropyl bromide
2-(4-methoxyphenyl)-3-methylbutyronitrile
Conditions | Yield |
---|---|
With sodium hydroxide; triethylamine In water | 98.7% |
With sodium hydroxide In benzene | 81% |
With sodium hydroxide In benzene | 81% |
benzaldehyde
p-methoxybenzylnitrile
(Z)-2-(4-methoxyphenyl)-3-phenylpropenenitrile
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol | 98% |
With sodium methylate In methanol at 30℃; Kinetics; Thermodynamic data; ΔE*, ς*, A; | 95% |
With sodium methylate In ethanol at 20℃; for 2h; | 93% |
Conditions | Yield |
---|---|
With dihydrogen peroxide; potassium carbonate In dimethyl sulfoxide for 0.333333h; Ambient temperature; | 98% |
With Os(hydride)6(triisopropylphosphine)2; water In tetrahydrofuran-d8 at 100℃; for 24h; Inert atmosphere; | 95% |
With tetra(n-butyl)ammonium hydroxide In ethanol; water at 80℃; for 8h; Green chemistry; chemoselective reaction; | 90% |
cyclohexanone
p-methoxybenzylnitrile
1-[cyano(4-methoxyphenyl)methyl]cyclohexanol
Conditions | Yield |
---|---|
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In methanol at 25 - 30℃; for 6h; | 98% |
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate at 0 - 15℃; for 1h; | 97% |
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In water at 0 - 15℃; for 2.2h; | 97.6% |
p-methoxybenzylnitrile
allyl bromide
diphenyldisulfane
2-(4-Methoxy-phenyl)-2-phenylsulfanyl-pent-4-enenitrile
Conditions | Yield |
---|---|
With potassium hydroxide | 98% |
2-Aminonicotinaldehyde
p-methoxybenzylnitrile
2-amino-3-(p-methoxyphenyl)-1,8-naphthyridine
Conditions | Yield |
---|---|
With piperidine at 20℃; for 0.133333h; | 98% |
With potassium hydroxide Microwave irradiation; | |
With piperidine In neat (no solvent) at 20℃; |
p-methoxybenzylnitrile
benzyl alcohol
2-(4-methoxyphenyl)-3-phenylpropanenitrile
Conditions | Yield |
---|---|
With potassium tert-butylate; C35H27Cl2N4PRuS In toluene at 135℃; for 1h; Inert atmosphere; Schlenk technique; | 98% |
With C41H44ClIrN2O4; potassium hydroxide In toluene at 135℃; for 2h; Reagent/catalyst; | 96% |
With potassium hydroxide; [IrCP*Cl2]2 at 100℃; for 16h; | 93% |
Conditions | Yield |
---|---|
With sodium methylate In methanol; ethanol at 20℃; for 0.166667h; Knoevenagel Condensation; | 98% |
Conditions | Yield |
---|---|
With sodium methylate In methanol; ethanol at 20℃; for 0.166667h; Knoevenagel Condensation; | 98% |
Conditions | Yield |
---|---|
With sodium methylate In methanol; ethanol at 20℃; for 0.166667h; Knoevenagel Condensation; | 98% |
methyl 2,4-bis(benzyloxy)-5-bromobenzoate
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
Stage #1: p-methoxybenzylnitrile With lithium hexamethyldisilazane In tetrahydrofuran at -78℃; for 0.5h; Inert atmosphere; Stage #2: methyl 2,4-bis(benzyloxy)-5-bromobenzoate In tetrahydrofuran at -78 - 20℃; for 2h; Inert atmosphere; | 97.2% |
Stage #1: p-methoxybenzylnitrile With lithium hexamethyldisilazane In tetrahydrofuran at -78℃; for 0.5h; Inert atmosphere; Stage #2: methyl 2,4-bis(benzyloxy)-5-bromobenzoate In tetrahydrofuran at -78 - 20℃; for 2.5h; Inert atmosphere; | 97.2% |
p-methoxybenzylnitrile
ethyl 2-(4-methoxyphenyl)acetimidate hydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride In ethanol at 4℃; for 72h; | 97% |
With hydrogenchloride In ethanol | |
With hydrogenchloride In ethanol at 0 - 5℃; |
ethyl iodide
p-methoxybenzylnitrile
2-ethyl-2-(4-methoxyphenyl)butanenitrile
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide; mineral oil at 20℃; for 20h; Cooling with ice; | 97% |
Conditions | Yield |
---|---|
With C26H50N6Zn2 In neat (no solvent) at 60℃; Schlenk technique; Glovebox; | 97% |
With Os(hydride)6(triisopropylphosphine)2 In (2)H8-toluene; 1,3,5-trimethyl-benzene at 60℃; for 48h; Sealed tube; Inert atmosphere; | 69% |
With [κ2-{2-F-C6H4NP(Se)Ph2}2Al(Me)] In neat (no solvent) at 60℃; for 10h; Schlenk technique; Glovebox; Inert atmosphere; chemoselective reaction; | 80 %Spectr. |
p-methoxybenzylnitrile
Conditions | Yield |
---|---|
With tetra(n-butyl)ammonium hydroxide In ethanol for 2h; Reflux; | 97% |
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