Formaldehyde → 4-(2-Bromo-2,2-difluoro-ethyl)-1-hydroxymethyl-pyrrolidin-2-one
反応式
[Br:1][C:2]([F:11])([F:10])[CH2:3][CH:4]1[CH2:8][NH:7][C:6](=[O:9])[CH2:5]1.[CH2:12]=[O:13]>C[Si](Cl)(C)C>[Br:1][C:2]([F:10])([F:11])[CH2:3][CH:4]1[CH2:8][N:7]([CH2:12][OH:13])[C:6](=[O:9])[CH2:5]1参加物
4
実験手順
In a 50 ml three necked flask fitted with a magnetic stirrer, under inert atmosphere, a solution of 4-(2-bromo-2,2-difluoro-ethyl)-pyrrolidin-2-one a6 (0.46 g, 2 mmol), paraformaldehyde (0.12 g) and TMSCl (10 ml) is heated at 60° C. for 1 h. The reaction mixture is evaporated to give the crude 4-(2-bromo-2,2-difluoro-ethyl)-1-hydroxymethyl-pyrrolidin-2-one a7 (0.48 g, 92%).
後処理
- customThe reaction mixture is evaporated
出典と根拠
- ORDレコード
- ord-5dd6a68815664df9be35bc92fc49b330
- 出典データセット
- uspto-grants-2010_07
- 特許番号
- US07763644B2
反応ノート
読み込み中…