Diethyl Ether → 4-(2-Bromoacetyl)-4-phenylpiperidine hydrobromide
反応式
[Br:1]Br.Cl.[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:1][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
8 g of bromine are added rapidly at RT to a suspension of 11.98 g of 4-acetyl-4-phenylpiperidine hydrochloride in 200 ml of DCM, and the reaction mixture is left stirring overnight at RT. It is diluted by adding 200 ml of ether, and the precipitate formed is drained and washed with ether. 17.88 g of the expected product are obtained after drying under vacuum.
後処理
- waitthe reaction mixture is left
- additionIt is diluted
- customthe precipitate formed
- washwashed with ether
出典と根拠
- ORDレコード
- ord-7e9dc4906751498b9c07a52496974797
- 出典データセット
- uspto-grants-1998_11
- 特許番号
- US05830906
反応ノート
読み込み中…