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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287963Generated: October 25, 2026

Ethanol → HCID 21503217, compound

https://huagongshe.com/reaction/1287963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantVinyltriethoxysilaneHCID 6516—
ReactantChlorodiphenylphosphineHCID 66180—
ReactantVinylsilaneHCID 81714—
ReactantSodiumHCID 5360545—
SolventTolueneHCID 1140—
ProductDiphenylphosphineHCID 7001716.3%
ProductHCID 21503217HCID 2150321716.7%

Reaction Steps

To a suspension of sodium diphenylphosphide prepared, under nitrogen in dry toluene (100 ml), from sodium (4.6, 0.2 g atom) and diphenylphosphinous chloride (22.0 g, 0.1 mol), vinyl triethoxysilane (19.0 g, 0.1 mol) is added during 45 minutes. A slight temperature rise occurs. The temperature is held at 30° C by adjusting the feed rate of the vinyl silane. After 3 hours, 5 ml anhydrous ethanol is added. The yellow color of the anion is instantly discharged. The solution is filtered to remove inorganic salts. Gas chromatographic analysis confirms the presence of diphenyl phosphine and 2-(dipenylphosphinyl)ethyl triethoxysilane. After neutralization with carbon dioxide, the liquid is distilled giving 6.3 g (16.7 percent yield) of 2-(diphenylphosphinyl) ethyl triethoxysilane and 3.0 g (16.3 percent yield) of diphenylphosphine. The H'NMR spectrum of the silane is identical to that of the product of addition of diphenylphosphine to vinyl triethoxysilane with a radical initiator.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03987009
Source datasetuspto-grants-1976_10
ORD IDord-3a1a5d85b97544fc8c317f13b16ea707
Source noteuspto-grants-1976_10