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Potassium Hydroxide → 3-(1-((Tert-butoxy)carbonyl)piperidin-4-yl)propanoic acid

HRID 2185564
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HRID 2185564 반응식
[OH-].[K+].C([O:5][C:6](=[O:22])[CH2:7][CH2:8][CH:9]1[CH2:14][CH2:13][N:12]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:11][CH2:10]1)C>O.CCO>[C:18]([O:17][C:15]([N:12]1[CH2:13][CH2:14][CH:9]([CH2:8][CH2:7][C:6]([OH:22])=[O:5])[CH2:10][CH2:11]1)=[O:16])([CH3:21])([CH3:19])[CH3:20]
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참가 물질

5

반응물 2

HCID 14797Potassium HydroxideHCID 23245138Tert-butyl 4-(3-ethoxy-3-oxopropyl)piperidine-1-carboxylate

생성물 1

HCID 15125403-(1-((Tert-butoxy)carbonyl)piperidin-4-yl)propanoic acid

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

A solution of KOH (86%, 0.42 g, 6.4 mmol) in water (1.5 mL) was added to a solution of 3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propionic acid ethyl ester in 95% EtOH (15 mL) at rt. After 2.5 h, the mixture was partitioned between EtOAc (50 mL) and 2 N aq. HCl (50 mL). After extraction of the aqueous layer with EtOAc (50 mL), the organic layers were washed with sat'd NaCl (25 mL), dried (Na2SO4), decanted, and evaporated to give 1.06 g of the title compound as a crystalline solid.

후처리

  1. customthe mixture was partitioned between EtOAc (50 mL) and 2 N aq. HCl (50 mL)
  2. extractionAfter extraction of the aqueous layer with EtOAc (50 mL)
  3. washthe organic layers were washed with sat'd NaCl (25 mL)
  4. dry with materialdried (Na2SO4)
  5. customdecanted
  6. customevaporated

출처 및 근거

ORD 기록
ord-84ac710993d7447f9f634083b8ed4d4f
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06399619B1

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