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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 21055322, 화합물 → HCID 21055323, 화합물

HRID 2215269
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HRID 2215269 반응식
[C:1]1([CH3:24])[CH:6]=[CH:5][C:4]([S:7]([O:10][CH2:11][C@@H:12]([CH2:22][CH3:23])[CH2:13][O:14]CC2C=CC=CC=2)(=[O:9])=[O:8])=[CH:3][CH:2]=1>[OH-].[Pd+2].[OH-].C(O)C>[C:1]1([CH3:24])[CH:2]=[CH:3][C:4]([S:7]([O:10][CH2:11][C@@H:12]([CH2:22][CH3:23])[CH2:13][OH:14])(=[O:8])=[O:9])=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 21055322HCID 21055322, 화합물

생성물 1

HCID 21055323HCID 21055323, 화합물수율 92%

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매HCID 702Ethanol용매

실험 절차

1.5 g (0.0043 mol) of 2-(S)-ethyl-3-benzyloxypropyl p-toluenesulfonate (XVIIId-1), 12 ml of ethanol and 0.29 g of 20% palladium hydroxide are introduced into a 100 ml round-bottomed flask. The mixture is vigorously stirred at ambient temperature under a slight hydrogen pressure. After reacting for one hour, the mixture is filtered through celite and the solid is washed with ethanol. The filtrate is concentrated under reduced pressure and the residue is purified by flash chromatography on silica gel (eluent: dichloromethane/cyclohexane=80:20). 1.02 g (0.0039 mol) of the title compound (XIXd-1) are recovered in the form of a colorless oil.

후처리

  1. filtrationthe mixture is filtered through celite
  2. washthe solid is washed with ethanol
  3. concentrationThe filtrate is concentrated under reduced pressure
  4. customthe residue is purified by flash chromatography on silica gel (eluent: dichloromethane/cyclohexane=80:20)

출처 및 근거

ORD 기록
ord-97114eff8f3b48e393819b4823cb6cbd
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07109234B2

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