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2-Deoxyribose, D- → 2-Deoxy-D-ribitol

HRID 481739
노트
인쇄 미리보기

반응식

HRID 481739 반응식
[O:1]=[CH:2][CH2:3][C@@H:4]([C@@H:6]([CH2:8][OH:9])[OH:7])[OH:5].[H][H]>O.[Ni]>[CH2:2]([OH:1])[CH2:3][C@@H:4]([C@@H:6]([CH2:8][OH:9])[OH:7])[OH:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 54600052-Deoxyribose, D-HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 107967912-Deoxy-D-ribitol

시약·촉매·용매 2

HCID 935Nickel촉매HCID 962Water용매

반응 조건

온도
70 °C

실험 절차

An 80 g (0.60 mole) portion of 2-deoxy-D-ribose was dissolved in 240 ml of water to form an aqueous solution into which 15 g of Raney nickel were added. The thus prepared reaction mixture in an autoclave was heated under a hydrogen pressure of 40 kg/cm2G up to a temperature of 70° C. taking 30 minutes and kept for additional 1 hour at the same temperature and under the same hydrogen pressure. After cooling, the reaction mixture taken out of the autoclave was filtered to remove the solid catalyst and the filtrate, as combined with the washings of the solid catalyst with water, was subjected to removal of the water to give about 80 g of 2-deoxy-D-erythropentitol. The yield of the product was almost quantitative.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. additionwere added
  2. customThe thus prepared reaction mixture in an autoclave
  3. temperatureAfter cooling
  4. filtrationwas filtered
  5. customto remove the solid catalyst
  6. customwas subjected to removal of the water

출처 및 근거

ORD 기록
ord-a95efa4b623d4ef6b6f30990f2bcdffb
출처 데이터셋
uspto-grants-1998_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05789572

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