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Methanol → HCID 57062068, 화합물

HRID 2289387
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HRID 2289387 반응식
CO.[CH3:3][C@H:4]([CH2:16][CH2:17][CH2:18][CH3:19])[CH2:5][C:6](=[O:15])[CH2:7][C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9]>C(Cl)Cl>[OH:15][C@@H:6]([CH2:5][C@H:4]([CH3:3])[CH2:16][CH2:17][CH2:18][CH3:19])[CH2:7][C:8]([O:10][C:11]([CH3:12])([CH3:13])[CH3:14])=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 887MethanolHCID 53727906HCID 53727906, 화합물

생성물 1

HCID 57062068HCID 57062068, 화합물수율 73%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

In a 200 ml autoclave were charged 50 ml of methanol, 14.0 g of t-butyl (R)-5-methyl-3-oxononanoate obtained in Step 5, and a solution of 0.49 g of (S)-di[2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]tetrachlorodiruthenium triethylamine in 40 ml of methylene chloride, and the mixture was allowed to react under a hydrogen pressure of 60 kg/cm2 for 18 hours. The solvent was removed by distillation under reduced pressure to obtain 13.6 g of a crude product, which was then purified by silica gel column chromatography to obtain 10.3 g (72.5%) of the titled compound.

후처리

  1. customto react under a hydrogen pressure of 60 kg/cm2 for 18 hours
  2. customThe solvent was removed by distillation under reduced pressure
  3. customto obtain 13.6 g of a crude product, which
  4. customwas then purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-151283faef6f49fc835b8bc8253a4238
출처 데이터셋
uspto-grants-2000_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06093345

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