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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463632Generated: October 29, 2026

Chlorotrimethylsilane → HCID 10093926, compound

https://huagongshe.com/reaction/1463632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantN-(2,3-Epoxypropyl)phthalimideHCID 21601—
ReactantHCID 178454912HCID 178454912—
CatalystZincchlorideHCID 3007855—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10093926HCID 10093926—

Reaction Steps

A mixture of 3.79 g of anhydrous triethylamine and 4.5 g ethyl n-butylphosphinate in 100 ml of anhydrous tetrahydrofuran under an inert atmosphere is treated with 4.07 g of trimethylchlorosilane. The resulting suspension is stirred for 20 hours at room temperature and the solid removed by filtration. Concentration in vacuo affords a cloudy, colourless oil which is treated with 6.09 g of anhydrous N-(2,3-epoxypropyl)phthalimide and 0.5 g of anhydrous zinc chloride. The mixture is heated to 66° C. under an inert atmosphere for 3 hours, cooled to 20° and diluted with dichloromethane. The organic solution is washed with 100 ml 10% of aqueous sodium bicarbonate solution and dried over anhydrous magnesium sulphate. Removal of the solvent and chromatography on silica gel affords ethyl 3-phthalimido-2-trimethylsilyloxy-propyl(n-butyl)phosphinate as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05300679
Source datasetuspto-grants-1994_04
ORD IDord-a2e208232e8e4e74a7e803144e9af83b
Source noteuspto-grants-1994_04