Hydrochloric Acid → 4-(3-Methylphenyl)piperidine hydrochloride

HRID 867017ノート

反応式

HRID 867017 の反応式
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

7

反応物 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 14797Potassium HydroxideHCID 203117071-Phenoxycarbonyl-4-(3-toluyl)piperidine

生成物 1

HCID 219369674-(3-Methylphenyl)piperidine hydrochloride

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 3283Diethyl Ether溶媒

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 salt 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

  1. temperatureat reflux for 24 hours
  2. customthe ethanol is partially removed
  3. extractionthe resulting mixture is extracted with ether
  4. extractionthe combined ether extracts are extracted with 1N HCl
  5. extractionextracted with ether
  6. dry with materialthe combined ether extracts are dried
  7. customthe ether is removed
  8. customleaving a dark oil
  9. customto produce the salt which
  10. filtrationis collected by filtration
  11. customdried
  12. customrecrystallized thrice from an ethanol-water mixture

出典と根拠

ORDレコード
ord-24fd22d7e19b4c0d876393a32703c8c2
出典データセット
uspto-grants-1978_07
特許番号
US04101663

反応ノート

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