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Epichlorohydrin → Sodium butyl 2-hydroxy-3chloropropyl phosphate

HRID 648788
ノート
印刷プレビュー

反応式

HRID 648788 の反応式
[P:1]([O-:9])([O-:8])([O:3][CH2:4][CH2:5][CH2:6][CH3:7])=[O:2].[OH-].[Na+:11].[CH2:12]([CH:14]1[O:16][CH2:15]1)[Cl:13]>>[P:1]([O-:9])([O:8][CH2:15][CH:14]([OH:16])[CH2:12][Cl:13])([O:3][CH2:4][CH2:5][CH2:6][CH3:7])=[O:2].[Na+:11]
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

4

反応物 3

HCID 7835EpichlorohydrinHCID 14798Sodium HydroxideHCID 12691398Butyl phosphate

生成物 1

HCID 86743212Sodium butyl 2-hydroxy-3chloropropyl phosphate収率 86.5%

反応条件

温度
70 °C

実験手順

20 g (0.13 moles) of monobutyl phosphate having a purity of 99% (AV1=360.6, AV2=721.3) was charged into a reactor, to which 129 ml of 1N sodium hydroxide aqueous solution was added and agitated at 70° C. to obtain uniform solution, at which the acid value of the reaction system was 46.7. While keeping the reaction system at 70° C., 59.2 g (0.64 moles) of epichlorohydrin was gradually dropped, followed by agitation at the temperature for 20 hours. The acid value of the reaction system was approximately zero, revealing that the conversion rate of the phosphoric monoester was almost 100%. The resulting product was collected by HPLC and the solvent was distilled off under reduced pressure to obtain 30.2 g (yield 86.5%) of sodium butyl 2-hydroxy-3-chloropropyl phosphate.

後処理

  1. additionwas added
  2. customto obtain uniform solution
  3. customat 70° C.
  4. customThe resulting product was collected by HPLC
  5. distillationthe solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-311f385075b44f298805aeb9e2116330
出典データセット
uspto-grants-1988_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04736051

反応ノート

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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