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Trifluoroacetic acid → 4-Methyl-4-(2-trifluoromethylphenoxy)piperidine

HRID 552142
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반응식

HRID 552142 반응식
C(OC([N:8]1[CH2:13][CH2:12][C:11]([CH3:25])([O:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[C:21]([F:24])([F:23])[F:22])[CH2:10][CH2:9]1)=O)(C)(C)C.FC(F)(F)C(O)=O>ClCCl>[CH3:25][C:11]1([O:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[C:21]([F:24])([F:22])[F:23])[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 671718194-Methyl-4-(2-trifluoromethylphenoxy)piperidine-1-carboxylic acid tert-butyl ester

생성물 1

HCID 671715074-Methyl-4-(2-trifluoromethylphenoxy)piperidine

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a stirred solution of 4-methyl-4-(2-trifluoromethylphenoxy)piperidine-1-carboxylic acid tert-butyl ester (0.025 g, 0.070 mmol) in dichloromethane (5 mL) was added trifluoroacetic acid (1 mL). The resulting mixture was stirred at ambient temperature for 24 hours and then quenched with saturated aqueous solution of Na2CO3 (5 mL). The organic phase was washed with water (10 mL), saturated NaCl (10 mL), dried over MgSO4 and then concentrated in vacuo. The crude title compound was obtained and used without further purification.

후처리

  1. customquenched with saturated aqueous solution of Na2CO3 (5 mL)
  2. washThe organic phase was washed with water (10 mL), saturated NaCl (10 mL)
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-63d80397926a40ca8e30cb3a9c6ab492
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07951805B2

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