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

Hydrogen Bromide → Phosphonic acid, (3-bromo-2-hydroxypropyl)-, diethyl ester

HRID 2051965
ノート
印刷プレビュー

反応式

HRID 2051965 の反応式
[BrH:1].[O:2]1[CH2:13][CH:3]1[CH2:4][P:5](=[O:12])([O:9][CH2:10][CH3:11])[O:6][CH2:7][CH3:8]>>[Br:1][CH2:13][CH:3]([OH:2])[CH2:4][P:5](=[O:12])([O:9][CH2:10][CH3:11])[O:6][CH2:7][CH3:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 260Hydrogen BromideHCID 98446Diethyl 2,3-epoxypropylphosphonate

生成物 1

HCID 10934659Phosphonic acid, (3-bromo-2-hydroxypropyl)-, diethyl ester収率 86.1%

実験手順

(1)-(a) 47% Aqueous hydrobromic acid (82.8 g) was added dropwise to diethyl 2,3-epoxypropylphosphonate (77.6 g) under ice-cooling and with stirring over a five minutes interval. After the stirring was continued for an hour under ice-cooling and for 3 hours at ambient temperature, the reaction mixture was extracted with ethyl acetate (500 ml). The ethyl acetate layer was separated, washed three times with saturated aqueous sodium bicarbonate solution (200 ml and 100 ml×2) and twice with saturated aqueous sodium chloride solution (100 ml×2), dried over magnesium sulfate and evaporated to dryness to give oily diethyl 3-bromo-2-hydroxypropylphosphonate (94.7 g)

後処理

  1. temperaturecooling
  2. wait
After the stirring was continued for an hour under ice-
  • extractionthe reaction mixture was extracted with ethyl acetate (500 ml)
  • customThe ethyl acetate layer was separated
  • washwashed three times with saturated aqueous sodium bicarbonate solution (200 ml and 100 ml×2)
  • dry with materialtwice with saturated aqueous sodium chloride solution (100 ml×2), dried over magnesium sulfate
  • customevaporated to dryness
  • 出典と根拠

    ORDレコード
    ord-723919546f16475dafe7641549e30166
    出典データセット
    uspto-grants-1980_01
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04182758

    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