Diethyl Ether → 4-(2-Bromoacetyl)-4-phenylpiperidine hydrobromide
反応式
[Br:1]Br.[BrH:3].[C:4]([C:7]1([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:12][CH2:11][NH:10][CH2:9][CH2:8]1)(=[O:6])[CH3:5].CCOCC>C(Cl)Cl>[BrH:1].[Br:3][CH2:5][C:4]([C:7]1([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:8][CH2:9][NH:10][CH2:11][CH2:12]1)=[O:6]参加物
5
実験手順
7.9 g of bromine are added rapidly at RT to a suspension of 14 g of 4-acetyl-4-phenylpiperidine hydrobromide in 200 ml of DCM and the reaction mixture is stirred overnight at RT. It is diluted by the addition of 200 ml of ether and the precipitate formed is wrung and washed with ether to give 16.7 g of the expected product after drying under vacuum.
後処理
- customthe precipitate formed
- washwashed with ether
出典と根拠
- ORDレコード
- ord-e00921bfd75e4c38a3e801d76412bc7d
- 出典データセット
- uspto-grants-2001_06
- 特許番号
- US06242637B1
反応ノート
読み込み中…