Phosphorus pentachloride → Benzyl [2-(chlorosulfonyl)ethyl]carbamate
反応式
[CH2:1]([O:8][C:9]([NH:11][CH2:12][CH2:13][S:14]([OH:17])(=O)=[O:15])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.P(Cl)(Cl)(Cl)(Cl)[Cl:19]>C1(C)C=CC=CC=1>[CH2:1]([O:8][C:9]([NH:11][CH2:12][CH2:13][S:14]([Cl:19])(=[O:17])=[O:15])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
4
実験手順
2-(N-benzyloxycarbonylamino)ethanesulfonic acid (0.6 g; 2.31 mmol) was suspended in dry toluene (6 mL) and PCl5 was added (0.65 g; 3.11 mmol). The mixture was refluxed for 2 h, until complete dissolution of the reagents. After cooling at room temperature, the solvent was evaporated off under vacuum to give the crude 2-(N-benzyloxycarbonylamino)-ethanesulfonyl chloride pure enough for the next step.
後処理
- temperatureThe mixture was refluxed for 2 h, until complete dissolution of the reagents
- customthe solvent was evaporated off under vacuum
出典と根拠
- ORDレコード
- ord-96dad23c22f14b7aba9bdc59f93a87dd
- 出典データセット
- uspto-grants-2005_04
- 特許番号
- US06881755B2
反応ノート
読み込み中…