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Isopropanol → [Hydroxy(ethyl)phosphinyl]acetic acid

HRID 1028263
ノート
印刷プレビュー

反応式

HRID 1028263 の反応式
[CH2:1]([P:3]([CH2:6][CH2:7][OH:8])(=[O:5])[OH:4])[CH3:2].CC(C)=[O:11].OS(O)(=O)=O.O=[Cr](=O)=O.C(O)(C)C>CC(C)=O>[CH2:1]([P:3]([OH:4])([CH2:6][C:7]([OH:11])=[O:8])=[O:5])[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 3

HCID 3776IsopropanolHCID 46832563HCID 46832563、化合物HCID 131709961Jones' reagent

生成物 1

HCID 15357685[Hydroxy(ethyl)phosphinyl]acetic acid収率 81%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

13.8 g (0.1 mol) of ethyl-(2-hydroxyethyl)phosphinic acid (produced as in Example 8) in 500 ml of acetone were admixed with 0.11 mol of Jones reagent (12.7 g of chromium trioxide in 36.7 ml of water and 11.0 ml of concentrated sulfuric acid) at 0° C. by dropwise addition. The reaction mixture was additionally stirred for 3½ hours with ice cooling and for 1 hour at room temperature. After 12 ml of isopropanol have been added, the mixture is poured onto ice-water. Volatile constituents are subsequently distilled off in vacuo. The residue was taken up in tetrahydrofuran and extracted. Insoluble salts were filtered off. The solvent of the filtrate was removed in vacuo and the residue was recrystallized from acetone to obtain 12.3 g (81% of theory) of 2-(ethylhydroxyphosphinyl)acetic acid as colorless solid.

後処理

  1. additionthe mixture is poured onto ice-water
  2. distillationVolatile constituents are subsequently distilled off in vacuo
  3. extractionextracted
  4. filtrationInsoluble salts were filtered off
  5. customThe solvent of the filtrate was removed in vacuo
  6. customthe residue was recrystallized from acetone

出典と根拠

ORDレコード
ord-cbdc633ecbea4f15bd399a8c718cdee8
出典データセット
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08735476B2

反応ノート

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