2-(2-Hydroxyethyl)pyridine → 2-(2-Chloroethyl)pyridine
反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][CH2:8]O.O=S(Cl)[Cl:12]>C(Cl)Cl>[Cl:12][CH2:8][CH2:7][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=1参加物
4
実験手順
2-(Pyridin-2-yl)ethanol (1 g, 8.12 mmol) was first treated with SOCl2 (3 ml) in CH2Cl2 (10 ml) at rt for 3 hrs. The solvent was removed to get a crude 2-(2-chloroethyl)pyridine. Then following General Procedure A, the title compound (1.69 g, 79%) was prepared from 2-amino-4-chlorobenzenethiol (1.6 g, 9.74 mmol), K2CO3 (3.36 g, 24.36 mmol) in DMF (20 ml).
後処理
- customThe solvent was removed
出典と根拠
- ORDレコード
- ord-3aa0fdd955c24a93a593eeba40de6a24
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08877804B2
反応ノート
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