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Trifluoroacetic acid → (R)-5-[3-(trifluoromethyl)phenyl]pyrrolidin-2-one

HRID 1972238
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반응식

HRID 1972238 반응식
C(OC([N:8]1[C@@H:12]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([C:19]([F:22])([F:21])[F:20])[CH:14]=2)[CH2:11][CH:10](C(O)=O)[C:9]1=[O:26])=O)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[F:22][C:19]([F:20])([F:21])[C:15]1[CH:14]=[C:13]([C@@H:12]2[NH:8][C:9](=[O:26])[CH2:10][CH2:11]2)[CH:18]=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 59485976(5R)-1-(tert-butoxycarbonyl)-5-[3-(trifluoromethyl)phenyl]-2-oxopyrrolidine-3-carboxylic acid

생성물 1

HCID 59485901(R)-5-[3-(trifluoromethyl)phenyl]pyrrolidin-2-one

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

The mixture of (5R)-1-(tert-butoxycarbonyl)-5-[3-(trifluoromethyl)phenyl]-2-oxopyrrolidine-3-carboxylic acid obtained in Step E (ca. 1.21 mmol) and 30% TFA in DCM (6 mL) is stirred at rt for 30 min. The reaction mixture is then dissolved in DCM (120 mL), washed with saturated aq. NaHCO3 (40 mL) and brine (40 mL) and dried over Na2SO4. Concentration to give (R)-5-[3-(trifluoromethyl)phenyl]pyrrolidin-2-one as a slight brown solid (278 mg, 100% overall yield for two steps). This product is used for the next step without further purification. HPLC-MS calculated for C11H10F3NO (M+H+) 230.07, found 230.00.

후처리

  1. washwashed with saturated aq. NaHCO3 (40 mL) and brine (40 mL)
  2. dry with materialdried over Na2SO4
  3. concentrationConcentration
  4. customto give

출처 및 근거

ORD 기록
ord-09a7e11bf02f416eb21a6f6d2c2415cc
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08431607B2

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