反応式
[C:1]1([NH:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:13][S:14](O)(=[O:16])=[O:15]>>[CH2:11]([O:10][C:8](=[O:9])[NH:7][C:1]1[CH:6]=[CH:5][C:4]([S:14]([Cl:13])(=[O:16])=[O:15])=[CH:3][CH:2]=1)[CH3:12]参加物
3
反応条件
- 温度
- 60 °C
実験手順
To a stirred solution of chlorosulfonic acid (20 ml) at 0° C., was added N-phenylurethane (9.90 g) at such a rate that the temperature did not exceed 20° C. The reaction was then heated at 60° C. for 3 hours, cooled to ambient temperature and poured carefully onto ice. The resultant precipitate was collected by filtration and dried in vacuo to give (4-chlorosulfonyl-phenyl)-carbamic acid ethyl ester (14.50 g) as an off-white solid. LC-MS (METHOD B): RT=3.11 minutes, 284.23 (M+H)+.
後処理
- customdid not exceed 20° C
- temperaturecooled to ambient temperature
- additionpoured carefully onto ice
- filtrationThe resultant precipitate was collected by filtration
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-193f8b39b2fb4ac7b90f7b62d37db764
- 出典データセット
- uspto-grants-2005_05
- 特許番号
- US06897208B2
関連ノート
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