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Methanol → HCID 20363198、化合物

HRID 917833
ノート
印刷プレビュー

反応式

HRID 917833 の反応式
[S:1]([C:5]1[C:6]([O:8][C:9](=[O:11])[CH:10]=1)=[O:7])([OH:4])(=[O:3])=[O:2].[CH3:12][O-:13].[Na+:14].C[OH:16]>>[CH3:12][O:13][CH:10]([CH:5]([S:1]([OH:4])(=[O:3])=[O:2])[C:6]([O-:16])=[O:7])[C:9]([O-:8])=[O:11].[Na+:14].[Na+:14].[Na+:14]
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

4

反応物 3

HCID 887Methanol2 回HCID 10942334Sodium MethoxideHCID 12479880Sulfomaleic anhydride

生成物 1

HCID 20363198HCID 20363198、化合物

反応条件

温度
80 °C

実験手順

Sulfomaleic anhydride, 3.9 gm, was dissolved in 25 ml of methanol and refluxed for 5 hours. Then, 24 gm of 25% sodium methoxide in methanol was added and the solution was refluxed for 2 hours. The methanol was then evaporated and the residue was dissolved in 100 ml of water and heated for 1 hour at 80°C. The solution was then decolorized with 5 gm of charcoal, filtered and evaporated. The crude residue of trisodium α-methoxy-β-sulfosuccinate was purified by trituration with acetic acid and then filtered, washed with acetone and dried.

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. temperaturerefluxed for 5 hours
  2. temperaturethe solution was refluxed for 2 hours
  3. customThe methanol was then evaporated
  4. dissolutionthe residue was dissolved in 100 ml of water
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude residue of trisodium α-methoxy-β-sulfosuccinate was purified by trituration with acetic acid
  8. filtrationfiltered
  9. washwashed with acetone
  10. customdried

出典と根拠

ORDレコード
ord-91a9424586b9476994f2771bec7e074e
出典データセット
uspto-grants-1976_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03968110

反応ノート

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