Lithium Hydroxide → benzyl (3R,4R)-3-fluoro-4-hydroxypiperidine-1-carboxylate

HRID 1926649노트

반응식

HRID 1926649 반응식
[F:1][C@H:2]1[C@H:7]([O:8]CC2C=CC([N+]([O-])=O)=CC=2)[CH2:6][CH2:5][N:4]([C:19]([O:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[O:20])[CH2:3]1.[Li+].[OH-].CCOC(C)=O>C1COCC1.O>[F:1][C@H:2]1[C@H:7]([OH:8])[CH2:6][CH2:5][N:4]([C:19]([O:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[O:20])[CH2:3]1

참가 물질

5

반응물 3

HCID 3939Lithium HydroxideHCID 8857Ethyl AcetateHCID 68668648Benzyl trans-3-fluoro-4-[(4-nitrobenzyl)oxy]piperidine-1-carboxylate

생성물 1

HCID 52324488benzyl (3R,4R)-3-fluoro-4-hydroxypiperidine-1-carboxylate

시약·촉매·용매 1

HCID 21881883Oxolane--water (1/1)용매

실험 절차

To a solution of benzyl trans-3-fluoro-4-[(4-nitrobenzyl)oxy]piperidine-1-carboxylate (180 g, 0.45 mol) in THF/H2O (1500 mL) was added LiOH (39 g, 0.9 mol) in portions at 0° C. After the addition, the reaction mixture was allowed to warm to room temperature and stirred overnight. TLC (EtOAc:petroleum ether=1:2) showed the starting material was consumed completely. The reaction mixture was extracted with EtOAc (3×500 mL). The combined organic layers were washed with brine (800 mL), dried over anhydrous Na2SO4 and concentrated to a crude residue. The residue was purified by column chromatography (EtOAc:petroleum ether=1:20) to afford benzyl trans-3-fluoro-4-hydroxypiperidine-1-carboxylate as a white solid.

후처리

  1. additionAfter the addition
  2. customwas consumed completely
  3. extractionThe reaction mixture was extracted with EtOAc (3×500 mL)
  4. washThe combined organic layers were washed with brine (800 mL)
  5. dry with materialdried over anhydrous Na2SO4
  6. concentrationconcentrated to a crude residue
  7. customThe residue was purified by column chromatography (EtOAc:petroleum ether=1:20)

출처 및 근거

ORD 기록
ord-259e7a01d3f04cbea62e282ab8dd8f4c
출처 데이터셋
uspto-grants-2012_05
특허 번호
US08183245B2

반응 노트

불러오는 중…