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 to stand overnight at RT, with stirring. It is diluted by the addition of 200 ml of ether and the precipitate formed is filtered off and washed with ether to give 17.88 g of the expected product after drying under vacuum.
後処理
- waitthe reaction mixture is left
- customthe precipitate formed
- filtrationis filtered off
- washwashed with ether
出典と根拠
- ORDレコード
- ord-dc51313e419d4eada0def3647e473f64
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06710042B2
反応ノート
読み込み中…