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Acrylonitrile → Ethyl(2-cyanoethyl)phosphinic acid

HRID 576008
ノート
印刷プレビュー

反応式

HRID 576008 の反応式
[CH2:1]([P:3]([OH:5])[OH:4])[CH3:2].[C:6](#[N:9])[CH:7]=[CH2:8].[O-]S(OOS([O-])(=O)=O)(=O)=O.[Na+].[Na+]>O>[CH2:1]([P:3]([CH2:8][CH2:7][C:6]#[N:9])(=[O:5])[OH:4])[CH3:2]
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 3

HCID 7855AcrylonitrileHCID 62655Sodium PersulfateHCID 13411864Ethylphosphonous acid

生成物 1

HCID 46929271Ethyl(2-cyanoethyl)phosphinic acid収率 83%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
100 °C

実験手順

564 g (6 mol) of ethylphosphonous acid (produced as in Example 1) are dissolved in 860 g of water and initially charged to a 5 l five-neck flask equipped with thermometer, reflux condenser, high-performance stirrer and dropping funnel. The reaction mixture is heated to 100° C. and 371 g (7 mol) of acrylonitrile and 500 g of a 5% sodium peroxodisulfate solution (1.5 mol % based on acrylonitrile) are added dropwise at atmospheric pressure. Then, the water is distilled off, and the residue is taken up in THF, extracted and filtered. The solvent of the filtrate is removed in vacuo to leave 732 g (83% of theory) of ethyl(2-cyanoethyl)phosphinic acid as oil.

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. additioninitially charged to a 5 l five-neck flask
  2. customequipped with thermometer
  3. temperaturereflux condenser, high-performance stirrer
  4. distillationThen, the water is distilled off
  5. extractionextracted
  6. filtrationfiltered
  7. customThe solvent of the filtrate is removed in vacuo

出典と根拠

ORDレコード
ord-8c087ff8509648dcae71cd92a1e1d70f
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09035088B2

反応ノート

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