Benzoyl chloride → 3-Chloro-2,2,3-trifluoro-propionyl chloride
反応式
[Cl:1][CH:2]([F:9])[C:3]([F:8])([F:7])[C:4](O)=[O:5].C([Cl:18])(=O)C1C=CC=CC=1>>[Cl:1][CH:2]([F:9])[C:3]([F:8])([F:7])[C:4]([Cl:18])=[O:5]参加物
3
実験手順
In a three-necked 2 l flask provided with a Vigreux column, a condenser, and a collecting flask were brought 325 g (2 moles) of 3-chloro-2,2,3-trifluoro-propionic acid (Org.Synth.Coll. 5, 239) and 562 g (4 moles) of benzoyl chloride. The mixture was heated so that the acid chloride distilled over slowly. The collected product was refluxed for 20 min to eliminate any residual hydrochloric acid. Finally the product was distilled at normal pressure. Yield: 280 g. Boiling point: 72°-74° C.
後処理
- customIn a three-necked 2 l flask provided with a Vigreux column, a condenser, and a collecting flask
- distillationdistilled over slowly
- temperatureThe collected product was refluxed for 20 min
- distillationFinally the product was distilled at normal pressure
出典と根拠
- ORDレコード
- ord-c436943872e143dca8a6cbf920ea371e
- 出典データセット
- uspto-grants-1982_07
- 特許番号
- US04341864
反応ノート
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