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Trifluoroacetic acid → 3-(R)-(3-fluorobenzyl)pyrrolidine

HRID 927982
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반응식

HRID 927982 반응식
FC(F)(F)C(O)=O.[F:8][C:9]1[CH:10]=[C:11]([CH:25]=[CH:26][CH:27]=1)[CH2:12][C@@H:13]1[CH2:17][CH2:16][N:15](C(OC(C)(C)C)=O)[CH2:14]1>C(Cl)Cl>[F:8][C:9]1[CH:10]=[C:11]([CH:25]=[CH:26][CH:27]=1)[CH2:12][C@@H:13]1[CH2:17][CH2:16][NH:15][CH2:14]1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 71006943tert-butyl (R)-3-(3-fluorobenzyl)pyrrolidine-1-carboxylate2회

생성물 1

HCID 863184933-(R)-(3-fluorobenzyl)pyrrolidine수율 121.7%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Trifluoroacetic acid (10 mL) was added to a solution of tert butyl (R)-3-(3-fluorobenzyl)-pyrrolidine-1-carboxylate (Intermediate 99, 0.515 g) in DCM (10 mL) and the mixture was stirred for 1 hour at room temperature. The mixture was evaporated to dryness and the residue was partitioned between DCM and saturated aqueous NaHCO3. The organic extract was separated, dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give 3-(R)-(3-fluoro-benzyl)pyrrolidine (0.402 g) as an oil.

후처리

  1. customThe mixture was evaporated to dryness
  2. customthe residue was partitioned between DCM and saturated aqueous NaHCO3
  3. extractionThe organic extract
  4. customwas separated
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. customThe filtrate was evaporated to dryness

출처 및 근거

ORD 기록
ord-9b1b0b3733e54e85933a36e9ecd6bded
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09290472B2

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