Hydrogen chloride-ethyl acetate → 4-Cyano-4-(2-methylphenoxymethyl)piperidine hydrochloride
反応式
C(OC([N:8]1[CH2:13][CH2:12][C:11]([C:23]#[N:24])([CH2:14][O:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[CH3:22])[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:25].C(OCC)(=O)C>>[ClH:25].[C:23]([C:11]1([CH2:14][O:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[CH3:22])[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1)#[N:24]参加物
3
実験手順
After adding 10 ml of 4N hydrogen chloride/ethyl acetate to 273 mg of 1-(tert-butoxycarbonyl)-4-cyano-4-(2-methylphenoxymethyl)piperidine, the mixture was stirred for 6 hours at room temperature. The solvent was distilled off under reduced pressure to obtain 336 mg of 4-cyano-4-(2-methylphenoxymethyl)piperidine hydrochloride.
後処理
- distillationThe solvent was distilled off under reduced pressure
出典と根拠
- ORDレコード
- ord-c2dc2ec185664b2ca2152f471e5794f2
- 出典データセット
- uspto-grants-2006_02
- 特許番号
- US06995144B2
反応ノート
読み込み中…