Bromine → 1-(1-Acetylpiperidin-4-yl)-2-bromoethan-1-one
反応式
[N:1]1([C:10](=[O:12])[CH3:11])[CH2:6][CH2:5][CH:4]([C:7](=[O:9])[CH3:8])[CH2:3][CH2:2]1.[Br:13]Br>CO>[C:10]([N:1]1[CH2:6][CH2:5][CH:4]([C:7](=[O:9])[CH2:8][Br:13])[CH2:3][CH2:2]1)(=[O:12])[CH3:11]参加物
4
実験手順
In a 1000 mL flask, 1,1′-(piperidine-1,4-diyl)diethanone (38.0 g, 225 mmol) was dissolved in methanol (700 mL) and bromine (12.1 mL, 236 mmol) was added. After agitating for 3 hours the solvent was removed in vacuo. The resulting solid was washed with ethyl acetate, then distributed between ethyl acetate and sodium carbonate. The organic phase was separated, washed with brine, dried and evaporated to give the title compound.
後処理
- customwas removed in vacuo
- washThe resulting solid was washed with ethyl acetate
- customThe organic phase was separated
- washwashed with brine
- customdried
- customevaporated
出典と根拠
- ORDレコード
- ord-1b241b13d0d54244b9caf410ba9038c1
- 出典データセット
- uspto-grants-2013_01
- 特許番号
- US08362037B2
反応ノート
読み込み中…