Thionyl Chloride → 4-(6-Bromohexyloxy)benzoyl chloride
反応式
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][O:8][C:9]1[CH:17]=[CH:16][C:12]([C:13](O)=[O:14])=[CH:11][CH:10]=1.S(Cl)([Cl:20])=O>>[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][O:8][C:9]1[CH:17]=[CH:16][C:12]([C:13]([Cl:20])=[O:14])=[CH:11][CH:10]=1参加物
3
実験手順
A mixture of 452 g of 4-(6-bromohexyloxy)benzoic acid and 1000 g of thionyl chloride was stirred at room temperature for about 20 hours. The reaction mixture was concentrated in vacuo and residual thionyl chloride removed by repeated addition of toluene and concentration in vacuo. The oily product comprising 4-(6-bromohexyloxy)benzoyl chloride (450 ml) was used directly in the next reaction.
後処理
- concentrationThe reaction mixture was concentrated in vacuo and residual thionyl chloride
- customremoved
- additionaddition of toluene and concentration in vacuo
- customThe oily product comprising 4-(6-bromohexyloxy)benzoyl chloride (450 ml) was used directly in the next reaction
出典と根拠
- ORDレコード
- ord-b57962b008124058811d7136199c57ea
- 出典データセット
- uspto-grants-1990_07
- 特許番号
- US04939267
反応ノート
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