Sodium hydride → HCID 19860794, 화합물

HRID 1165736노트

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HRID 1165736 반응식
[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]

참가 물질

5

실험 절차

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.

후처리

  1. temperatureheating
  2. customthe resulting reaction mixture

출처 및 근거

ORD 기록
ord-96d8e8262de9448db68813441b04f9b6
출처 데이터셋
uspto-grants-1990_03
특허 번호
US04911887

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