反応式
[F:1][C:2]([F:17])([F:16])[C:3]1[CH:4]=[C:5]([C:9]2(O)[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)[CH:6]=[CH:7][CH:8]=1.[ClH:18]>O>[ClH:18].[F:17][C:2]([F:1])([F:16])[C:3]1[CH:4]=[C:5]([C:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH:10]=2)[CH:6]=[CH:7][CH:8]=1参加物
4
実験手順
In a round-bottomed flask equipped with a mechanical stirrer, 50 g of 4-(3-trifluoromethylphenyl)-4-piperidinol are charged to 377 ml of water and 514 ml of concentrated hydrochloric acid. The mixture is left to react at reflux for 5 hours and is then cooled to ambient temperature. A white solid precipitates. It is filtered off through a Büchner funnel and dried in an oven. 37 g of a white solid are isolated. M.p. 203-204° C.
後処理
- customIn a round-bottomed flask equipped with a mechanical stirrer
- waitThe mixture is left
- customto react
- temperatureat reflux for 5 hours
- customA white solid precipitates
- filtrationIt is filtered off through a Büchner funnel
- customdried in an oven
出典と根拠
- ORDレコード
- ord-8d33625c1f5646a4be3f592063add37e
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08193190B2
関連ノート
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