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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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ethyl(E)-3-(3'-methylaminobiphenyl-4-yl)acrylate → Ethyl 3-(3'-methylaminobiphenyl-4-yl)propanoate

HRID 250833
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인쇄 미리보기

반응식

HRID 250833 반응식
[CH3:1][NH:2][C:3]1[CH:4]=[C:5]([C:9]2[CH:14]=[CH:13][C:12](/[CH:15]=[CH:16]/[C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:11][CH:10]=2)[CH:6]=[CH:7][CH:8]=1>CO.[Pd]>[CH3:1][NH:2][C:3]1[CH:4]=[C:5]([C:9]2[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:11][CH:10]=2)[CH:6]=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 67272952ethyl(E)-3-(3'-methylaminobiphenyl-4-yl)acrylate

생성물 1

HCID 67271940Ethyl 3-(3'-methylaminobiphenyl-4-yl)propanoate수율 90%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A solution of 1.7 g (6.0 mmol) of ethyl (E)-3-(3′-methylaminobiphenyl-4-yl)acrylate in 25 ml of methanol is stirred for 12 hours at room temperature in the presence of 300 mg (18% by mass) of 10% palladium-on-charcoal under a hydrogen atmosphere. The palladium is filtered off and the solvent is evaporated off. 1.52 g of ethyl 3-(3′-methylaminobiphenyl-4-yl)propanoate are obtained. Yield=90%

후처리

  1. filtrationThe palladium is filtered off
  2. customthe solvent is evaporated off

출처 및 근거

ORD 기록
ord-6bbc2830869c405497b33ab1f27ac865
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07863332B2

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