Hydrochloric Acid → 4-(3-Methylphenyl)piperidine hydrochloride
反応式
O(C([N:10]1[CH2:15][CH2:14][CH:13]([C:16]2[CH:17]=[C:18]([CH3:22])[CH:19]=[CH:20][CH:21]=2)[CH2:12][CH2:11]1)=O)C1C=CC=CC=1.[OH-].[K+].O.[ClH:26]>C(O)C.CCOCC>[ClH:26].[C:18]1([CH3:22])[CH:19]=[CH:20][CH:21]=[C:16]([CH:13]2[CH2:12][CH2:11][NH:10][CH2:15][CH2:14]2)[CH:17]=1参加物
実験手順
A solution of 11.9 g of 1-phenoxycarbonyl-4-(3-toluyl)piperidine and 75 ml of an aqueous 50% potassium hydroxide solution in 300 ml of ethanol is heated at reflux for 24 hours and then stirred at ambient temperature for an additional 36 hours. 100 ml of water are added, the ethanol is partially removed, the resulting mixture is extracted with ether and the combined ether extracts are extracted with 1N HCl. The aqueous solution is basified with an aqueous sodium hydroxide solution, extracted with ether, the combined ether extracts are dried, and the ether is removed, leaving a dark oil. The oil is dissolved in ether and ethereal hydrogen chloride is added to produce the sale which is collected by filtration, dried and recrystallized thrice from an ethanol-water mixture to give 4-(3-toluyl)piperidine hydrochloride, mp 196°-197° C.,
後処理
- temperatureat reflux for 24 hours
- customthe ethanol is partially removed
- extractionthe resulting mixture is extracted with ether
- extractionthe combined ether extracts are extracted with 1N HCl
- extractionextracted with ether
- dry with materialthe combined ether extracts are dried
- customthe ether is removed
- customleaving a dark oil
- customto produce the sale which
- filtrationis collected by filtration
- customdried
- customrecrystallized thrice from an ethanol-water mixture
出典と根拠
- ORDレコード
- ord-16fe2b8288ba48178209a75f6fffad90
- 出典データセット
- uspto-grants-1977_09
- 特許番号
- US04046900
反応ノート
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