Methyl chloroformate → Benzoic acid, 4-(1-methylethenyl)-, methyl ester

HRID 362475

反応式

HRID 362475 の反応式
Cl[C:2]1[CH:10]=[CH:9][C:5]([C:6]([CH3:8])=[CH2:7])=[CH:4][CH:3]=1.[Mg].Cl[C:13]([O:15][CH3:16])=[O:14]>C1COCC1>[C:6]([C:5]1[CH:9]=[CH:10][C:2]([C:13]([O:15][CH3:16])=[O:14])=[CH:3][CH:4]=1)([CH3:8])=[CH2:7]

参加物

5

実験手順

Preparation of the Grignard compound of 4-chloro-α-methylstyrene by means of Rieke magnesium in THF under reflux and subsequent reaction with 0.95 equivalents of methyl chloroformate at RT. Aqueous working up, extraction with ethyl acetate and column chromatography using cyclohexane/ethyl acetate 85:15 affords methyl 4-isopropenylbenzoate as colorless crystals.

後処理

  1. temperatureunder reflux
  2. extractionextraction with ethyl acetate and column chromatography

出典と根拠

ORDレコード
ord-b9804facfb484b00bae18c748b7636e4
出典データセット
uspto-grants-1999_02
特許番号
US05869531

関連ノート

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