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Potassium Hydroxide → 4-Phenyl-4-(4-trifluoromethylphenoxy)piperidine

HRID 437580
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반응식

HRID 437580 반응식
O(C([N:10]1[CH2:15][CH2:14][C:13]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)([O:16][C:17]2[CH:22]=[CH:21][C:20]([C:23]([F:26])([F:25])[F:24])=[CH:19][CH:18]=2)[CH2:12][CH2:11]1)=O)C1C=CC=CC=1.[OH-].[K+]>C(O)C>[C:27]1([C:13]2([O:16][C:17]3[CH:18]=[CH:19][C:20]([C:23]([F:26])([F:24])[F:25])=[CH:21][CH:22]=3)[CH2:12][CH2:11][NH:10][CH2:15][CH2:14]2)[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 21428717HCID 21428717, 화합물

생성물 1

HCID 212682524-Phenyl-4-(4-trifluoromethylphenoxy)piperidine

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

A sample of 7.4 g of 1-phenoxycarbonyl-4-phenyl-4-(p-trifluoromethylphenoxy)piperidine is dissolved in 70 ml. of ethanol and 48 ml. of 45% aqueous KOH added, and the solution is stirred and refluxed under nitrogen for 4 hours. After cooling most of the ethanol is removed under reduced pressure and the resultant oily dispersion is extracted with ether. The ether was dried and then evaporated under reduced pressure to give a waxy, white solid of 4-phenyl-4(p-trifluoromethylphenoxy)piperidine.

후처리

  1. temperaturerefluxed under nitrogen for 4 hours
  2. customis removed under reduced pressure
  3. extractionthe resultant oily dispersion is extracted with ether
  4. dry with materialThe ether was dried
  5. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-5ab33bc04e034b34937482b0dc901776
출처 데이터셋
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04031221

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