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Ethyl 3-(2-methoxy-5-(methoxycarbonyloxy)phenyl)acrylate → Ethyl 3-(2-methoxy-5-(methoxycarbonyloxy)phenyl)propanoate

HRID 709695
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인쇄 미리보기

반응식

HRID 709695 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([O:9][C:10]([O:12][CH3:13])=[O:11])=[CH:5][C:4]=1[CH:14]=[CH:15][C:16]([O:18][CH2:19][CH3:20])=[O:17]>CO.[Pd]>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([O:9][C:10]([O:12][CH3:13])=[O:11])=[CH:5][C:4]=1[CH2:14][CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 131733903Ethyl 3-(2-methoxy-5-(methoxycarbonyloxy)phenyl)acrylate

생성물 1

HCID 117759608Ethyl 3-(2-methoxy-5-(methoxycarbonyloxy)phenyl)propanoate수율 79.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of ethyl 3-(2-methoxy-5-(methoxycarbonyloxy)phenyl)acrylate (1.00 g) in methanol (3.0 mL) was added 10% palladium-activated carbon (100 mg), and the mixture was stirred for 1 hr under a hydrogen atmosphere. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure to give the title compound (800 mg) as a yellow oil. This compound was used for the next step without further purification.

후처리

  1. filtrationThe reaction mixture was filtered
  2. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-9f60aaef950545d28b98ed2dc547e371
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181186B2

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