4-(1-Cyclohexen-1-yl)-3-(trifluoromethyl)benzamide → 4-Cyclohexyl-3-(trifluoromethyl)benzamide
反応式
[C:1]1([C:7]2[CH:15]=[CH:14][C:10]([C:11]([NH2:13])=[O:12])=[CH:9][C:8]=2[C:16]([F:19])([F:18])[F:17])[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]=1>CO.[Pd]>[CH:1]1([C:7]2[CH:15]=[CH:14][C:10]([C:11]([NH2:13])=[O:12])=[CH:9][C:8]=2[C:16]([F:17])([F:18])[F:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1参加物
4
実験手順
4-(1-Cyclohexen-1-yl)-3-(trifluoromethyl)benzamide (D32) (850 mg, 3.16 mmol) was dissolved in methanol (63 ml) and hydrogenated using an H-Cube, using palladium on carbon at 40° C. with a flow rate of 2 mL/min. The solvent was removed in vacuo to give the title compound as a white solid (822 mg). MS (ES): C14H16F3NO requires 271; found 272 (MH+).
後処理
- customat 40° C.
- customThe solvent was removed in vacuo
出典と根拠
- ORDレコード
- ord-9aaee2c39372469aad834e8d62aced5b
- 出典データセット
- uspto-grants-2012_12
- 特許番号
- US08324254B2
反応ノート
読み込み中…