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2-Deoxyribose, D- → 2-Deoxy-D-ribitol

HRID 481739
ノート
印刷プレビュー

反応式

HRID 481739 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 54600052-Deoxyribose, D-HCID 178418361HCID 178418361、化合物

生成物 1

HCID 107967912-Deoxy-D-ribitol

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 962Water溶媒

反応条件

温度
70 °C

実験手順

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.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  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

出典と根拠

ORDレコード
ord-a95efa4b623d4ef6b6f30990f2bcdffb
出典データセット
uspto-grants-1998_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05789572

反応ノート

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