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 s
Cas:13472-00-9
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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
Cas:13472-00-9
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Cas:13472-00-9
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inquiryProduct Name: 2-(4-Aminophenyl)ethylamine Synonyms: Benzeneethanamine, 4-amino-;beta-[4-Aminophenyl]ethylamine;4-(ETHYLAMINO)ANILINE;4-AMINO-BETA-PHENYLETHYLAMINE;4-AMINOPHENETHYLAMINE;4-(2-AMINOETHYL)ANILINE;4-(2-AMINO-ETHYL)-PHENYLAM
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inquiryOur advantages: 1. All inquiries will be replied within 12 hours. 2. Dedication to quality, supply & service. 3. Strictly on selecting raw materials. 4. Reasonable & competitive price, fast lead time. 5. Sample is available for your eva
Cas:13472-00-9
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
Cas:13472-00-9
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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
Cas:13472-00-9
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inquiry1,we produce and sell good chemicals around the world. 2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%. 3,our staff consists of highly qualifie
Cas:13472-00-9
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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inquiryBest quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At present
Cas:13472-00-9
Min.Order:1 Gram
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Type:Trading Company
inquiryCompany Introduction 1. Established in 2005, with two independent business divisions: Fine chemicals division; Pharmaceutical division. 2. Main product: Optical brightener Textile auxiliary Dye stuff Pigments
Cas:13472-00-9
Min.Order:1 Gram
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inquiryJ&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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inquiryA substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
Cas:13472-00-9
Min.Order:4 Kilogram
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Cas:13472-00-9
Min.Order:100 Gram
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inquiryEstablished in May 2015, TaiChem Ltd. is initially invested by a British research and development company and started by PhDs back from aboard. The company is registered in China Medical City (CMC), Taizhou, Jiangsu Province, and the production site
Cas:13472-00-9
Min.Order:10 Gram
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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 providing h
Product name: 2-(4-Aminophenyl)Ethylamine CAS No.: 13472-00-9 Molecule Formula:C8H13N2 Molecule Weight:137.20 Purity: 99.0% Package: 25kg/drum Description:White crystalline powder Manufacture Standards:Enterprise Standard TESTING
Cas:13472-00-9
Min.Order:1 Kilogram
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inquiryCangzhou 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 api, intermediat
Cas:13472-00-9
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FOB Price: $5.0 / 15.0
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inquiryProduct 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,
Cas:13472-00-9
Min.Order:1 Kilogram
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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,
Cas:13472-00-9
Min.Order:1 Milligram
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inquiryProduct Name: 2-(4-Aminophenyl)ethylamine CAS: 13472-00-9 MF: C8H12N2 MW: 136.19 EINECS: 236-739-2 Mol File: 13472-00-9.mol 2-(4-Aminophenyl)ethylamine Structure 2-(4-Aminophenyl)ethylamine Chemical Properties Melting point 28
Cas:13472-00-9
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryZhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed
Cas:13472-00-9
Min.Order:1 Kilogram
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
Hangzhou Hysen pharma CO.,LTD. is a professional Pharmaceutical company. We are specialized in manufacturing and R&D of API & Intermediates, Contract Manufacturing, Contract Research, and International Trading business as well. *We ow
Cas:13472-00-9
Min.Order:1 Gram
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Type:Lab/Research institutions
inquiryStock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
Cas:13472-00-9
Min.Order:0
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inquiryHangzhou Dingyan Chem is a leading manufacturer and supplier of chemicals in China.We develop,produce and distribute high quality pharmaceuticals, intermediates, special chemicals and other fine chemicals.Appearance:A white or almost white crystallin
Cas:13472-00-9
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inquiryhigh purity,in stock Package:25kg/drum,or as per customers'demand Application:API,Pharmaceutical intermediates Transportation:air,sea,courier
Cas:13472-00-9
Min.Order:0
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inquiryAcmec is a leading manufacturer and supplier of biochemical reagents and life science products. We have over 40,000 items in stock (real-time inventory) and offer discounted prices to registered members of the online store ( www.acmec.com.cn ) Appea
Cas:13472-00-9
Min.Order:1 bottle
Negotiable
Type:Lab/Research institutions
inquiryhigh quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
p-aminophenylacetonitrile
p-Aminophenethylamine
Conditions | Yield |
---|---|
With hydrazine hydrate; nickel In ethanol at 50 - 55℃; | 100% |
With hydrazine hydrate; nickel In ethanol at 50 - 55℃; Product distribution; Other aminoarylalkylnitriles. Object: selective reduction of the nitrile group.; | 100% |
With methanol; cobalt(II) chloride; diborane for 0.5h; Ambient temperature; | 97.7% |
2-(p-nitrophenyl)ethylamine
p-Aminophenethylamine
Conditions | Yield |
---|---|
With hydrogen In methanol at 20℃; under 760.051 Torr; | 100% |
With 5%-palladium/activated carbon; hydrogen In ethanol under 760.051 Torr; | 91% |
With hydrogenchloride; tin | |
With palladium on activated charcoal; hydrogen | |
With palladium on activated charcoal; hydrogen |
1-nitro-4-(2-nitroethyl)benzene
p-Aminophenethylamine
Conditions | Yield |
---|---|
With samarium diiodide; water; isopropylamine In tetrahydrofuran | 86% |
4-Nitrophenylacetonitrile
p-Aminophenethylamine
Conditions | Yield |
---|---|
With sodium tetrahydroborate; (-) In ethanol at 20℃; for 156h; | 77% |
With acetic anhydride; platinum Hydrogenation.Erhitzen des Reaktionsprodukts mit wss.Salzsaeure; | |
With ethanol; nickel Hydrogenation; |
1-azido-2-(4'-nitrophenyl)ethane
p-Aminophenethylamine
Conditions | Yield |
---|---|
With hydrogenchloride; indium In tetrahydrofuran at 20℃; for 7h; | 63% |
N-benzyloxycarbonyl-4-nitrophenethylamine
A
p-Aminophenethylamine
B
N-benzyloxycarbonyl-4-aminophenethylamine
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal; ethylenediamine In tetrahydrofuran at 20℃; under 760 Torr; for 8h; Hydrogenation; | A n/a B 60% C n/a |
(p-aminophenyl)alanine
p-Aminophenethylamine
Conditions | Yield |
---|---|
With pyridoxal 5'-phosphate; aromatic L-amino acid decarboxylase In various solvent(s) at 30℃; for 48h; | 28% |
N-<2-(4-nitrophenyl)ethyl>phthalimide
p-Aminophenethylamine
Conditions | Yield |
---|---|
With sodium sulfide; water |
4-(2-(((methyl)carbonyl)amino)ethyl)aniline
p-Aminophenethylamine
Conditions | Yield |
---|---|
With hydrogenchloride |
N-<2-(4-nitrophenyl)ethyl>acetamide
p-Aminophenethylamine
Conditions | Yield |
---|---|
With hydrogenchloride; tin; ethanol nachfolgendes Eindampfen; | |
Multi-step reaction with 2 steps 1: iron; aq.-ethanolic HCl 2: aqueous HCl View Scheme | |
With iron; acetic acid Eindampfen der alkalisch gemachten Loesung; |
p-aminophenylacetonitrile
cyclohexanol
A
p-Aminophenethylamine
B
(4-amino-phenethyl)-cyclohexyl-amine
C
bis-(4-amino-phenethyl)-amine
Conditions | Yield |
---|---|
at 90℃; Hydrogenation; |
ethanol
4-Nitrophenylacetonitrile
ethyl acetate
p-Aminophenethylamine
Conditions | Yield |
---|---|
at 20℃; |
tetralin
4-Nitrophenylacetonitrile
A
p-Aminophenethylamine
B
bis-(4-amino-phenethyl)-amine
Conditions | Yield |
---|---|
at 130℃; under 20 Torr; Hydrogenation; |
p-Aminophenethylamine
Conditions | Yield |
---|---|
With hydrogenchloride; palladium Hydrogenation.Behandeln des Reaktionsprodukts mit Kaliumcarbonat in wss.Natronlauge; | |
With hydrogenchloride; amalgamated zinc Behandeln des Reaktionsprodukts mit Kaliumcarbonat in wss.Natronlauge; | |
With hydrogenchloride; tin(ll) chloride Behandeln des Reaktionsprodukts mit Kaliumcarbonat in wss.Natronlauge; |
p-aminophenylacetonitrile
tetralin
A
p-Aminophenethylamine
B
bis-(4-amino-phenethyl)-amine
Conditions | Yield |
---|---|
at 130℃; Hydrogenation; |
2-(4-nitrophenyl)ethylamine monohydrochloride
p-Aminophenethylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 82 percent / Et3N / tetrahydrofuran / 17 h / 20 °C 2: H2 / Pd/C-ethylenediamine / tetrahydrofuran / 8 h / 20 °C / 760 Torr View Scheme | |
With palladium 10% on activated carbon; ammonium formate In methanol Reflux; |
methyl-N-(benzyl-methyl)-formamide
p-Aminophenethylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: tin; hydrochloric acid; alcohol / nachfolgendes Eindampfen View Scheme | |
Multi-step reaction with 2 steps 1: nitric acid / 0 °C 2: tin; hydrochloric acid; alcohol / nachfolgendes Eindampfen View Scheme |
phenethylamine
p-Aminophenethylamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 210 - 220 °C / durch Erhitzen zuletzt auf 290grad 3: tin; hydrochloric acid; alcohol / nachfolgendes Eindampfen View Scheme | |
Multi-step reaction with 3 steps 1: 210 - 220 °C / durch Erhitzen zuletzt auf 290grad 2: nitric acid / 0 °C 3: tin; hydrochloric acid; alcohol / nachfolgendes Eindampfen View Scheme | |
Multi-step reaction with 2 steps 1: hydrogenchloride; nitric acid / water / 20 °C 2: hydrogen; 5%-palladium/activated carbon / ethanol / 760.05 Torr View Scheme | |
Multi-step reaction with 2 steps 1: sulfuric acid; nitric acid 2: palladium on activated charcoal; hydrogen View Scheme |
(4-nitrophenyl)ethyl bromide
p-Aminophenethylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: potassium carbonate / 150 °C 2: sodium sulfide; water View Scheme |
1-phenyl-2-bromoethane
p-Aminophenethylamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: Nitrierung 2: potassium carbonate / 150 °C 3: sodium sulfide; water View Scheme | |
Multi-step reaction with 3 steps 1: glacial acetic acid; acetic acid anhydride; fuming nitric acid / <0 2: potassium carbonate / 150 °C 3: sodium sulfide; water View Scheme |
2-4-aminophenylethylcarbamic acid methyl ester
p-Aminophenethylamine
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid; trifluoroacetic acid at 70℃; Kinetics; Inert atmosphere; |
4-(2-aminoethyl)-N-(tert-butoxycarbonyl)phenylamine
p-Aminophenethylamine
Conditions | Yield |
---|---|
With trifluoroacetic acid In dichloromethane at 20℃; for 24h; Concentration; | 14.1 g |
2-(4-nitrophenyl)ethanol
p-Aminophenethylamine
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: hydrogen; palladium on activated charcoal / methanol / 12 h / 40 °C / 1500.15 Torr / Autoclave 2: triethanolamine / methanol / 12 h / 70 °C / Inert atmosphere 3: triethylamine / dichloromethane / 2 h / -5 - 20 °C 4: ammonium hydroxide / N,N-dimethyl-formamide / 5 h / 100 °C / Inert atmosphere 5: trifluoroacetic acid / dichloromethane / 24 h / 20 °C View Scheme | |
Multi-step reaction with 5 steps 1: hydrogen; palladium on activated charcoal / methanol / 12 h / 40 °C / 1500.15 Torr / Autoclave 2: triethanolamine / methanol / 12 h / 70 °C / Inert atmosphere 3: triethylamine / dichloromethane / 2 h / 10 - 20 °C 4: ammonium hydroxide / N,N-dimethyl-formamide / 5 h / 80 °C / Inert atmosphere 5: trifluoroacetic acid / dichloromethane / 24 h / 20 °C View Scheme |
2-(4'-aminophenyl)ethyl alcohol
p-Aminophenethylamine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: triethanolamine / methanol / 12 h / 70 °C / Inert atmosphere 2: triethylamine / dichloromethane / 2 h / -5 - 20 °C 3: ammonium hydroxide / N,N-dimethyl-formamide / 5 h / 100 °C / Inert atmosphere 4: trifluoroacetic acid / dichloromethane / 24 h / 20 °C View Scheme | |
Multi-step reaction with 4 steps 1: triethanolamine / methanol / 12 h / 70 °C / Inert atmosphere 2: triethylamine / dichloromethane / 2 h / 10 - 20 °C 3: ammonium hydroxide / N,N-dimethyl-formamide / 5 h / 80 °C / Inert atmosphere 4: trifluoroacetic acid / dichloromethane / 24 h / 20 °C View Scheme |
tert-butyl N-[4-(2-hydroxyethyl)phenyl]carbamate
p-Aminophenethylamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: triethylamine / dichloromethane / 2 h / -5 - 20 °C 2: ammonium hydroxide / N,N-dimethyl-formamide / 5 h / 100 °C / Inert atmosphere 3: trifluoroacetic acid / dichloromethane / 24 h / 20 °C View Scheme | |
Multi-step reaction with 3 steps 1: triethylamine / dichloromethane / 2 h / 10 - 20 °C 2: ammonium hydroxide / N,N-dimethyl-formamide / 5 h / 80 °C / Inert atmosphere 3: trifluoroacetic acid / dichloromethane / 24 h / 20 °C View Scheme |
p-Aminophenethylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: ammonium hydroxide / N,N-dimethyl-formamide / 5 h / 80 °C / Inert atmosphere 2: trifluoroacetic acid / dichloromethane / 24 h / 20 °C View Scheme |
4-(2-aminoethyl)benzenamine hydrochloride salt
p-Aminophenethylamine
Conditions | Yield |
---|---|
With sodium hydroxide In water | 0.51 g |
p-Aminophenethylamine
Conditions | Yield |
---|---|
With triethylamine In dichloromethane for 4h; | 100% |
p-Aminophenethylamine
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 20℃; | 100% |
p-Aminophenethylamine
α,α,α-trifluoro-o-diacetotoluidide
4-(2-(((methyl)carbonyl)amino)ethyl)aniline
Conditions | Yield |
---|---|
In ethanol at 0℃; | 98% |
p-Aminophenethylamine
di-tert-butyl dicarbonate
tert-butyl 4-aminophenethylcarbamate
Conditions | Yield |
---|---|
In 1,4-dioxane | 98% |
In tetrahydrofuran at 0 - 20℃; for 1h; | 98% |
With triethylamine In dichloromethane at 20 - 24℃; for 16h; Reagent/catalyst; Solvent; | 98% |
p-Aminophenethylamine
Allyl chloroformate
4-(2-aminoethyl)-N-(allylcarbonyloxy)phenylamine
Conditions | Yield |
---|---|
With acetic acid In 1,4-dioxane; water pH=4.5; regioselective reaction; | 98% |
With acetic acid In 1,4-dioxane; water at 20℃; | 69% |
p-Aminophenethylamine
1,3-diphenyl-2-propynone
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 20℃; for 5h; chemoselective reaction; | 98% |
p-Aminophenethylamine
2-(3-[N-tert-butoxycarbonylaminophenyl]amino)-4-chloro-6-cyclopentylamino-1,3,5-triazine
2-(2-[4-aminophenyl]ethylamino)-4-(3-[N-tert-butoxycarbonylaminophenyl]amino)-6-cyclopentylamino-1,3,5-triazine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 20 - 60℃; for 20h; | 97% |
p-Aminophenethylamine
4-maleimidobutyric acid N-hydroxysuccinimide ester
Conditions | Yield |
---|---|
In aq. phosphate buffer; N,N-dimethyl acetamide for 2h; pH=8; | 97% |
p-Aminophenethylamine
9-benzoyl-9H-carbazole
N-(4-aminophenethyl)benzamide
Conditions | Yield |
---|---|
In tetrahydrofuran at 30℃; for 24h; chemoselective reaction; | 97% |
p-Aminophenethylamine
C15H16ClNO4
7-methoxy-8-butyloxy-2-oxo-1,2-dihydroquinoline-3-carboxylic acid 2-(4-amino-phenyl)ethylamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 16h; | 96% |
p-Aminophenethylamine
2-[4-([3-tert-butoxycarobnylaminophenyl]amino)-6-[2-[4-[4-([3-tert-butoxycarbonylaminophenyl]amino)-6-chloro[1,3,5]triazine-2-ylamino]phenyl]ethylamino][1,3,5]triazine-2-ylamino]ethanol
Conditions | Yield |
---|---|
With hydrogenchloride In 1,4-dioxane | 95% |
p-Aminophenethylamine
benzyl chloroformate
4-(2-aminoethyl)-N-(benzyloxycarbonyl)phenylamine
Conditions | Yield |
---|---|
With acetic acid In 1,4-dioxane; water at 20℃; pH=4.5; regioselective reaction; | 93% |
at 20℃; regioselective reaction; | 81% |
p-Aminophenethylamine
3,5-di-tert-butylbenzoic acid
N-[2-(4-aminophenyl)ethyl]-3,5-di-tert-butyl-benzamide
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 25℃; for 16h; | 93% |
p-Aminophenethylamine
1-iodo-3-isocyanatobenzene
1-[2-(4-aminophenyl)ethyl]-3-(3-iodophenyl)urea
Conditions | Yield |
---|---|
In dichloromethane at 20℃; Cooling with ice; | 92% |
p-Aminophenethylamine
4-(N-maleimidomethyl)cyclohexane-1-carboxylic acid N-succinimidyl ester
Conditions | Yield |
---|---|
In aq. phosphate buffer; N,N-dimethyl acetamide for 2h; pH=8; | 92% |
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 120℃; for 20h; Temperature; | A 91.5% B 80.42 g |
p-Aminophenethylamine
2-(4-anilino-6-chloro-[1,3,5]triazin-2-ylamino)-ethanol
2-[2-(4-aminophenyl)ethylamino]-4-(2-hydroxyethylamino)-6-phenylamino-1,3,5-triazine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 60℃; for 20h; | 91% |
p-Aminophenethylamine
1-(phenylsulfonyl)-1H-benzo[d][1,2,3]triazole
Conditions | Yield |
---|---|
In tetrahydrofuran for 40h; Ambient temperature; | 90% |
p-Aminophenethylamine
N,N'-bis( tert-butoxycarbonyl)-1H-pyrazole-1-carboxamidine
Conditions | Yield |
---|---|
With acetic acid In 1,4-dioxane; water at 20℃; for 18h; | 90% |
p-Aminophenethylamine
(R)-2-hydroxy-2-phenylethyl 4-methylbenzenesulfonate
YM-208876
Conditions | Yield |
---|---|
In acetonitrile at 70℃; for 10h; | 89.7% |
p-Aminophenethylamine
1-acetoxy-4-methylbenzene
4-(2-(((methyl)carbonyl)amino)ethyl)aniline
Conditions | Yield |
---|---|
at 20℃; for 30h; | 89.7% |
at 20℃; for 30h; | 89.7% |
p-Aminophenethylamine
acrylonitrile
3-(4-aminophenethyl)aminopropionitrile
Conditions | Yield |
---|---|
With Ps-AlCl3 at 20℃; for 2h; Michael Addition; regioselective reaction; | 89% |
p-Aminophenethylamine
(R)-4-(oxiran-2-yl)-2,8-bis(trifluoromethyl)quinoline
Conditions | Yield |
---|---|
In ethanol at 130℃; for 0.5h; Microwave irradiation; | 89% |
p-Aminophenethylamine
(S)-4-(oxiran-2-yl)-2,8-bis(trifluoromethyl)quinoline
Conditions | Yield |
---|---|
In ethanol at 130℃; for 0.5h; Microwave irradiation; | 89% |
p-Aminophenethylamine
ethyl trifluoroacetate,
N-[2-(4-aminophenyl)ethyl]-2,2,2-trifluoroacetamide
Conditions | Yield |
---|---|
In chloroform at 0 - 20℃; for 16h; | 89% |
p-Aminophenethylamine
acrylic acid methyl ester
methyl 3-(4-aminophenethyl)aminopropanoate
Conditions | Yield |
---|---|
With Ps-AlCl3 at 20℃; for 2h; Michael Addition; regioselective reaction; | 88% |
p-Aminophenethylamine
5-bromo-1,3-xylene
Conditions | Yield |
---|---|
With tris(dibenzylideneacetone)dipalladium (0); potassium carbonate; XPhos In tert-butyl alcohol at 100℃; for 22h; | A n/a B 87% |
p-Aminophenethylamine
Conditions | Yield |
---|---|
With sodium azide; sulfuric acid; sodium nitrite In water at 0℃; for 0.333333h; | 87% |
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