反応式
[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH2:9][C:10]([OH:12])=O.S(Cl)([Cl:15])=O>>[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH2:9][C:10]([Cl:15])=[O:12]参加物
3
実験手順
28.3g (0.113 mol) of 2-bromo-p-chlorophenylacetic acid was mixed with 26.9g (0.226 mol) of thionylchloride and the mixture was refluxed for 2.5 hours. After the excess thionylchloride had been distilled off, the reaction mixture was distilled under reduced pressure to give 26.7g of 2-bromo-p-chlorophenylacetyl chloride as yellow-orange oil. (b.p. 148° - 152°C/15 mmHg)
後処理
- temperaturethe mixture was refluxed for 2.5 hours
- distillationAfter the excess thionylchloride had been distilled off
- distillationthe reaction mixture was distilled under reduced pressure
出典と根拠
- ORDレコード
- ord-0a9b9b78ae254be2987c42d7e132ee20
- 出典データセット
- uspto-grants-1976_07
- 特許番号
- US03971828
関連ノート
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