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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165736Generated: October 31, 2026

Sodium hydride → HCID 19860794, compound

https://huagongshe.com/reaction/1165736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,5-DiphosphonotetrahydrofuranHCID 14817555—
ReactantDimethylphosphiteHCID 21884954—
Solvent2,5-DimethoxytetrahydrofuranHCID 79098—
ProductHCID 19860794HCID 19860794—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04911887
Source datasetuspto-grants-1990_03
ORD IDord-96d8e8262de9448db68813441b04f9b6
Source noteuspto-grants-1990_03