反応式
[Br:1][CH:2]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])[C:3](O)=[O:4].S(Cl)([Cl:14])=O>C1(C)C=CC=CC=1>[Br:1][CH:2]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])[C:3]([Cl:14])=[O:4]参加物
4
実験手順
To a solution of 20 g (90 mmol) 2-bromooctanoic acid in 100 mL toluene was added 13.2 mL (180 mmol) thionyl chloride. The solution was heated at reflux under nitrogen for 3 hours. The excess thionyl chloride and toluene were distilled at atmospheric pressure under N2. The yellow residue was purified by kugelrohr distillation (bp=60°-65° C./0.1 mm Hg) and 13.8 g (64%) of the 2-bromooctanoyl chloride as a colorless oil was isolated.
後処理
- temperatureThe solution was heated
- temperatureat reflux under nitrogen for 3 hours
- distillationThe excess thionyl chloride and toluene were distilled at atmospheric pressure under N2
- distillationThe yellow residue was purified by kugelrohr distillation (bp=60°-65° C./0.1 mm Hg)
出典と根拠
- ORDレコード
- ord-acd63c64178a4462a306cbb7bbee6c9f
- 出典データセット
- uspto-grants-1995_05
- 特許番号
- US05420305
関連ノート
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