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

HRID 1158127
ノート
印刷プレビュー

反応式

HRID 1158127 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

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)+.

後処理

  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)

出典と根拠

ORDレコード
ord-7244cb3929d24fabb49ea6f9b3be2a9b
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07807720B2

反応ノート

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