ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Acetone → (R)-isopropylidenebutane-1,2,4-triol

HRID 1087392
ノート
印刷プレビュー

反応式

HRID 1087392 の反応式
[CH2:1]([OH:7])[C@H:2]([OH:6])[CH2:3][CH2:4][OH:5].C(=O)(O)[O-].[Na+].[CH3:13][C:14]([CH3:16])=O>Cl(O)(=O)(=O)=O.O>[C:14](=[C:1]([OH:7])[C@H:2]([OH:6])[CH2:3][CH2:4][OH:5])([CH3:16])[CH3:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 180AcetoneHCID 516892Sodium BicarbonateHCID 69942791,2,4-Butanetriol, (2R)-

生成物 1

HCID 86744937(R)-isopropylidenebutane-1,2,4-triol収率 31%

試薬・触媒・溶媒 2

HCID 24247Perchloric Acid触媒HCID 962Water溶媒

実験手順

(R)-(+)-1,2,4-Butanetriol (0.7 g, 6.6 mmol), prepared as described in step a) above, was stirred for 1.5 h in acetone (50 ml) containing 3 drops of conc. perchloric acid, a satured solution of sodium bicarbonate in water (5 ml) was added and the stirring was continued for additional 10 min. The precipitate was filtered off and the filtrate evaporated under reduced pressure (2.7 kPa, 30° C.). The residue was taken up in ethyl acetate, washed with saturated aqueous sodium bicarbonate (5 ml) and brine (5 ml), and dried over magnesium sulphate. Evaporation of the solvent and distillation gave the title compound as a colourless oil (0.3 g, 2.05 mmol, 31%): b.p. 104°-106° C. at~2.7 kPa. nD20 =1.4390.

後処理

  1. filtrationThe precipitate was filtered off
  2. customthe filtrate evaporated under reduced pressure (2.7 kPa, 30° C.)
  3. washwashed with saturated aqueous sodium bicarbonate (5 ml) and brine (5 ml)
  4. dry with materialdried over magnesium sulphate
  5. customEvaporation of the solvent and distillation

出典と根拠

ORDレコード
ord-95dc4a34650b47ee84da867cb13429a5
出典データセット
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05036071

反応ノート

読み込み中…

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