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3-Methoxycarbonyl-2-(1-naphthylmethylene)propionic acid → 3-Methoxycarbonyl-2-(1-naphthylmethyl)propionic acid

HRID 1722907
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인쇄 미리보기

반응식

HRID 1722907 반응식
[CH3:1][O:2][C:3]([CH2:5][C:6](=[CH:10][C:11]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH:14]=[CH:13][CH:12]=1)[C:7]([OH:9])=[O:8])=[O:4]>CO.[Pd]>[CH3:1][O:2][C:3]([CH2:5][CH:6]([CH2:10][C:11]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH:14]=[CH:13][CH:12]=1)[C:7]([OH:9])=[O:8])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 543827543-Methoxycarbonyl-2-(1-naphthylmethylene)propionic acid

생성물 1

HCID 140953623-Methoxycarbonyl-2-(1-naphthylmethyl)propionic acid수율 98.9%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of 251 mg of the propionic acid compound in 10 ml of methyl alcohol was added 30 mg of a 10% palladium charcoal, and the mixture was hydrogenated under a hydrogen atmosphere at room temperature. After filtration of the catalyst, the reaction mixture was concentrated under reduced pressure to obtain 250 mg of 3-methoxycarbonyl-2-(1-naphthylmethyl)propionic acid as a white powder.

후처리

  1. customwas hydrogenated under a hydrogen atmosphere at room temperature
  2. filtrationAfter filtration of the catalyst
  3. concentrationthe reaction mixture was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-688cffc0842f42babee884432e3272df
출처 데이터셋
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04857650

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