反応式
[CH3:1][O:2][C:3]1[C:4]([F:14])=[C:5]([CH:9]=[C:10]([F:13])[C:11]=1[F:12])[C:6](O)=[O:7].S(Cl)([Cl:17])=O>C1C=CC=CC=1>[CH3:1][O:2][C:3]1[C:4]([F:14])=[C:5]([CH:9]=[C:10]([F:13])[C:11]=1[F:12])[C:6]([Cl:17])=[O:7]参加物
4
実験手順
To a solution of 1.14 g (0.0055 mole) of 3-methoxy-2,4,5-trifluorobenzoic acid (XXVI) (prepared as described in Preparation 1 or 2) in 10 ml of dry benzene was added 5 ml of thionyl chloride and the mixture was heated under reflux for 1 hour. At the end of this time, benzene and the excess of thionyl chloride were removed completely to give 3-methoxy-2,4,5-trifluorobenzoyl chloride (XXVII) [Step (E7)].
後処理
- temperaturethe mixture was heated
- temperatureunder reflux for 1 hour
- customAt the end of this time, benzene and the excess of thionyl chloride were removed completely
出典と根拠
- ORDレコード
- ord-e8340abe867a4d70b81c6228fb698fd8
- 出典データセット
- uspto-grants-1991_03
- 特許番号
- US04997943
関連ノート
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