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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376051Generated: November 1, 2026

Chlorotrimethylsilane → HCID 178476819, compound

https://huagongshe.com/reaction/376051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantEthyl chloroformateHCID 10928—
ReactantPhosphinic AcidHCID 4124402—
ReactantHCID 178460913HCID 178460913—
ReactantHCID 178476775HCID 178476775—
SolventAcetoneHCID 180—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 178476819HCID 178476819—

Reaction Steps

Hypophosphorous acid (100%, 2.0 g, 0.03M) and ethyl chloroformate (3.3 g, 0.03M) are stirred under nitrogen at room temperature in THF (40 ml). Triethylamine (3.03 g, 0.03M) is carefully added with cooling over 1 hour. 31P nmr shows that there is 85% conversion to ethyl hypophosphite (31P nmr δ=16 ppm). Trimethylsilyl chloride (3.3 g, 0.3M) is added followed by triethylamine (3.03 g, 0.03M). The mixture is stirred for 1 hour, when conversion to ethyltrimethylsilyl phosphinate (31P nmr δ=149 ppm) is complete. Acetone (5 ml) is added and the mixture is stirred for 1 hour at 60° C. The mixture is then cooled, quenched with water and washed with methylene chloride. The aqueous phase is evaporated and the residual gum is stirred with ether. Evaporation of the ether gives ethyl (1-hydroxy-1-methylethyl)phosphinate after distillation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05488171
Source datasetuspto-grants-1996_01
ORD IDord-997bd79b8ebb47db98978c40011094bf
Source noteuspto-grants-1996_01