反応式
S(Cl)([Cl:3])=O.[CH2:5]([O:15][C:16]1[CH:24]=[CH:23][C:19]([C:20](O)=[O:21])=[CH:18][CH:17]=1)[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]>CN(C)C=O.C(Cl)(Cl)(Cl)Cl>[CH2:5]([O:15][C:16]1[CH:24]=[CH:23][C:19]([C:20]([Cl:3])=[O:21])=[CH:18][CH:17]=1)[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]参加物
5
実験手順
A 300 ml two-necked flask equipped with a stirrer and a reflux condenser was charged with 100 ml of carbon tetrachloride, 4.5 ml of thionyl chloride and 11.1 g of 4-n-decyloxybenzoic acid obtained by a conventional method, and heated under reflux together with one drop of dimethylformamide for 4 hours. Then, unreacted thionyl chloride was removed under reduced pressure to obtain 4-decyloxybenzoyl chloride as a colorless liquid.
後処理
- customA 300 ml two-necked flask equipped with a stirrer and a reflux condenser
- customobtained by a conventional method
- temperatureheated
- customThen, unreacted thionyl chloride was removed under reduced pressure
出典と根拠
- ORDレコード
- ord-de8ea2b0bfca4db4a062d4e0f3d4eec8
- 出典データセット
- uspto-grants-1994_05
- 特許番号
- US05308536
関連ノート
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