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

HRID 2309151
ノート
印刷プレビュー

反応式

HRID 2309151 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

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 minute 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. waitAfter 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-1d7f1583dbcb41998194fa196e226ed6
    出典データセット
    uspto-grants-1987_09
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04693742

    反応ノート

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