Sodium hydride → HCID 19860794、化合物

HRID 1165736ノート

反応式

HRID 1165736 の反応式
[P:1]([CH:5]1[CH2:9][CH2:8][CH:7](P(O)(O)=O)[O:6]1)([OH:4])([OH:3])=[O:2].P([O-])(OC)[O:15][CH3:16].[H-].[Na+]>COC1CCC(OC)O1>[P:1]([CH:5]1[CH2:9][CH2:8][CH:7]([O:15][CH3:16])[O:6]1)([OH:4])([OH:3])=[O:2]

参加物

5

実験手順

To make 2,5-diphosphonotetrahydrofuran (i.e. n is 2), step (a) is suitably accomplished by adding dimethyl phosphite to a cool slurry of sodium hydride in 2,5-dimethoxytetrahydrofuran under an inert atmosphere such as nitrogen or argon and heating the resulting reaction mixture to form 2-phosphono-5-methoxytetrahydrofuran as a first intermediate. Step (b) is suitably accomplished by adding bromotrimethyl silane to said first intermediate and stirring the resulting mixture under an inert atmosphere such as nitrogen or argon, thereby forming di-(trimethylsilyl)2-phosphono-5-bromotetrahydrofuran as a second intermediate. Step (c) is suitably accomplished by adding triisopropyl phosphite to said second intermediate and heating the mixture under an inert atmosphere such as nitrogen or argon, thereby forming 2-(di-(trimethyl silyl)phosphono)-5-(diisopropylphosphono)-tetrahydrofuran. Diphosphonotetrahydrofuran may be produced by adding a concentrated acid, such as hydrochloric acid to the 2-(di-(trimethyl silyl)phosphono)-5-(diisopropylphosphono)-tetrahydrofuran and refluxing the acid solution. 2,6-Diphosphonotetrahydropyran (i.e. n is 3) and 2,7-Diphosphonooxepane (i.e. n is 4) may be produced in similar fashion, respectively using 2,6-dimethoxytetrahydropyran and 2,7-dimethoxyoxepane rather than 2,5-dimethoxytetrahydrofuran as a starting material.

後処理

  1. temperatureheating
  2. customthe resulting reaction mixture

出典と根拠

ORDレコード
ord-96d8e8262de9448db68813441b04f9b6
出典データセット
uspto-grants-1990_03
特許番号
US04911887

反応ノート

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