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Sodium Bicarbonate → tert-Butyl (3S)-3-fluoropyrrolidine-1-carboxylate

HRID 1445771
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HRID 1445771 반응식
COCCN(S(F)(F)[F:11])CCOC.[C:14]([N:21]1[CH2:25][CH2:24][C@@H:23](O)[CH2:22]1)([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15].C(=O)([O-])O.[Na+]>ClCCl>[F:11][C@H:23]1[CH2:24][CH2:25][N:21]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:22]1
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참가 물질

5

반응물 3

HCID 516892Sodium BicarbonateHCID 2734690(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 6544479tert-Butyl (3R)-3-hydroxypyrrolidine-1-carboxylate

생성물 1

HCID 18453464tert-Butyl (3S)-3-fluoropyrrolidine-1-carboxylate수율 81.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Slowly add [bis(2-methoxyethyl)amino]sulfur trifluoride (2.40 mL, 13.03 mmol) to a solution of N-Boc-(R)-(−)-3-pyrrolidinol (2.00 g, 10.86 mmol) in anhydrous dichloromethane (10 mL), at −78° C. and under nitrogen. Allow the reaction mixture to warm to room temperature and stir overnight. Carefully add an aqueous solution of sodium hydrogen carbonate (saturated, 20 mL) and extract with dichloromethane. Concentrate the combined organic extracts under vacuum then purify using automated flash chromatography (ISCO® System, 120 g Redisep® SiO2 column; 0-40% ethyl acetate in cyclohexane gradient elution over 30 minutes at 85 mL/min) to give the title compound as a pale yellow liquid (1.67 g): MS (m/e): 212 (M+23).

후처리

  1. customat −78° C.
  2. extractionextract with dichloromethane
  3. concentrationConcentrate the combined organic extracts under vacuum
  4. customthen purify
  5. washflash chromatography (ISCO® System, 120 g Redisep® SiO2 column; 0-40% ethyl acetate in cyclohexane gradient elution over 30 minutes at 85 mL/min)

출처 및 근거

ORD 기록
ord-b91f0bc6101b430d8fa5df236e3fe673
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07666871B2

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