1,3-Cyclohexanedione → 2-Bromocyclohexane-1,3-dione
反応式
[C:1]1(=[O:8])[CH2:6][CH2:5][CH2:4][C:3](=[O:7])[CH2:2]1.[Br:9]Br>CC(O)=O>[Br:9][CH:2]1[C:3](=[O:7])[CH2:4][CH2:5][CH2:6][C:1]1=[O:8]参加物
4
実験手順
To a stirred solution of cyclohexane-1,3-dione (1.12 g, 10 mmol) in AcOH (20 mL) at r.t. was added bromine (1.6 g, 0.51 mL, 10 mmol) dropwise. The reaction mixture was stirred for 2 h and then the product was isolated by filtration. The precipitate was washed twice with Et2O (100 mL) and then dried in vacuo to give the title compound in quantitative yield as a buff solid, which was used without further purification. LCMS (ES+) 190.9 (M+H)+.
後処理
- customthe product was isolated by filtration
- washThe precipitate was washed twice with Et2O (100 mL)
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-71186469f40b42658d4deaa0c35056b0
- 出典データセット
- uspto-grants-2011_02
- 特許番号
- US07888344B2
反応ノート
読み込み中…