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Ethyl 3-(4-fluoro-3,5-dimethylphenyl)-2-methylacrylate → Ethyl 2-(4-fluoro-3,5-dimethylbenzyl)propanoate

HRID 1158127
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HRID 1158127 반응식
[F:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([CH:9]=[C:10]([CH3:16])[C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:4][C:3]=1[CH3:17]>CO.[Pd]>[F:1][C:2]1[C:3]([CH3:17])=[CH:4][C:5]([CH2:9][CH:10]([CH3:16])[C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:6][C:7]=1[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 68642179Ethyl 3-(4-fluoro-3,5-dimethylphenyl)-2-methylacrylate

생성물 1

HCID 59512575Ethyl 2-(4-fluoro-3,5-dimethylbenzyl)propanoate수율 88%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of Ethyl 3-(4-fluoro-3,5-dimethylphenyl)-2-methylacrylate (0.190 g, 0.855 mmol) in 10 mL of MeOH, was added Pd (10 wt % on activated carbon, 0.038 g). After stirring at room temperature under H2 (1 atm) for 40 h, the reaction mixture was filtered through a pad of Celite and washed with MeOH. The filtrate was concentrated under reduced pressure. The crude product was used directly in the next step without further purification (0.138 g, 88% yield). LC-MS: tR=10.9 min; m/z 239 (M+H)+.

후처리

  1. filtrationthe reaction mixture was filtered through a pad of Celite
  2. washwashed with MeOH
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. customThe crude product was used directly in the next step without further purification (0.138 g, 88% yield)

출처 및 근거

ORD 기록
ord-7244cb3929d24fabb49ea6f9b3be2a9b
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07807720B2

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