Water → Ethyl 3-(4-fluorophenyl)acrylate

HRID 1506155

反応式

HRID 1506155 の反応式
[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.C(OP([CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20])(OCC)=O)C.[O-]CC.[Na+].C(O)C.O>O1CCCC1>[F:1][C:2]1[CH:9]=[CH:8][C:5](/[CH:6]=[CH:18]/[C:19]([O:21][CH2:22][CH3:23])=[O:20])=[CH:4][CH:3]=1

参加物

6

実験手順

4-Fluorobenzaldehyde (9.61 g, 80.0 mmol) in tetrahydrofuran (120 mL) was mixed with ethyl 2-(diethoxyphosphoryl)acetate (17.9 g, 80.0 mmol) under cooling with ice, and then sodium ethoxide-ethanol solution (21 wt %, 44.8 mL, 120 mmol) was added dropwise to the reaction mixture under cooling with ice, and the resulting reaction mixture was stirred at room temperature for 2 hours. After addition of water, the reaction mixture was extracted with ethyl acetate, and the organic layer dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=20/1→10/1 (v/v)) to give the title compound as a colorless oil (14.1 g, yield 91%).

後処理

  1. temperatureunder cooling with ice
  2. temperatureunder cooling with ice
  3. customthe resulting reaction mixture
  4. extractionthe reaction mixture was extracted with ethyl acetate
  5. dry with materialthe organic layer dried over anhydrous sodium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography (hexane/ethyl acetate=20/1→10/1 (v/v))

出典と根拠

ORDレコード
ord-a09054b200b64d068416ddf3a74431a4
出典データセット
uspto-grants-2015_12
特許番号
US09216999B2

関連ノート

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