Thionyl Chloride → 2-(2,6-Dichlorophenyl)acetyl chloride
反応式
S(Cl)([Cl:3])=O.[Cl:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([Cl:12])[C:7]=1[CH2:13][C:14]([OH:16])=O>C1(C)C=CC=CC=1>[Cl:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([Cl:12])[C:7]=1[CH2:13][C:14]([Cl:3])=[O:16]参加物
4
実験手順
30.93 g of thionyl chloride are added dropwise to a warmed, mechanically stirred mixture of 45.12 g of 2,6-dichlorophenylacetic acid in 125 ml of toluene. The reaction mixture is then maintained at reflux for 5 hrs and cooled overnight at RT. The reaction mixture is concentrated in vacuo and the concentrate dissolved in hot petroleum ether and the solids filtered. The filtrate is concentrated in vacuo to give a dark amber liquid, which is distilled to give a clear pinkish liquid.
後処理
- temperatureThe reaction mixture is then maintained
- temperatureat reflux for 5 hrs
- concentrationThe reaction mixture is concentrated in vacuo
- dissolutionthe concentrate dissolved in hot petroleum ether
- filtrationthe solids filtered
- concentrationThe filtrate is concentrated in vacuo
- customto give a dark amber liquid, which
- distillationis distilled
- customto give a clear pinkish liquid
出典と根拠
- ORDレコード
- ord-9c6f3cc32d0b4d0190c16567badbd980
- 出典データセット
- uspto-grants-1985_10
- 特許番号
- US04544670
反応ノート
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