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Ethanol → 3-O-Ethylascorbic acid

HRID 1175199
ノート
印刷プレビュー

反応式

HRID 1175199 の反応式
[CH2:1]([O:3][C:4]1[C@@H:9]([C@H:10]([C:12](=C(C)C)[OH:13])[OH:11])[O:8][C:6](=[O:7])[C:5]=1[OH:17])[CH3:2].C(O)C>O.Cl>[CH2:1]([O:3][C:4]1[C@@H:9]([C@H:10]([CH2:12][OH:13])[OH:11])[O:8][C:6](=[O:7])[C:5]=1[OH:17])[CH3:2]
参加物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 702EthanolHCID 66915691HCID 66915691、化合物

生成物 1

HCID 1507363-O-Ethylascorbic acid収率 84.3%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒HCID 962Water溶媒

実験手順

12.4 g of the 3-O-ethyl-isopropylidene ascorbic acid obtained in Example 1 was dissolved in 100 ml of distilled water, to which 10 ml of 2N hydrochloric acid solution was added. The mixture was reacted at 60° C. for 2 hours and concentrated under reduced pressure to give an adhesive liquid product. Ethanol was added to the prepared liquid product, which was then concentrated to give crude crystalline 3-ethyl-ascorbic acid. The crude crystalline 3-ethyl-ascorbic acid was re-crystallized in ethylacetate/ethanol (8:2) to give 8.6 g of white crystalline 3-O-ethyl-ascorbic acid (yield: 84.3%).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. additionwas added
  2. customThe mixture was reacted at 60° C. for 2 hours
  3. concentrationconcentrated under reduced pressure
  4. customto give an adhesive liquid product
  5. concentrationwas then concentrated
  6. customto give crude crystalline 3-ethyl-ascorbic acid
  7. customThe crude crystalline 3-ethyl-ascorbic acid was re-crystallized in ethylacetate/ethanol (8:2)

出典と根拠

ORDレコード
ord-1dbce865394346f88324c9844697df1c
出典データセット
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07838690B2

反応ノート

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