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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050727Generated: October 27, 2026

Chlorotrimethylsilane → Ethyl 3-phthalimido-2-trimethylsilyloxy-propyl(ethyl)phosphinate

https://huagongshe.com/reaction/2050727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantN-(2,3-Epoxypropyl)phthalimideHCID 21601—
ReactantHCID 178476785HCID 178476785—
CatalystZincchlorideHCID 3007855—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-phthalimido-2-trimethylsilyloxy-propyl(ethyl)phosphinateHCID 19090885—

Reaction Steps

A mixture of 4.55 g of anhydrous triethylamine and 5.0 g of ethyl ethylphosphinate in 100 ml of anhydrous tetrahydrofuran under an inert atmosphere is treated with 4.89 g of chlorotrimethylsilane. 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 5.10 g of anhydrous N-(2,3-epoxypropyl)phthalimide and 1.0 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 of a 10% aqueous sodium bicarbonate solution and dried over anhydrous magnesium sulphate. Removal of the solvents and chromatography on silica gel affords ethyl 3-phthalimido-2-trimethylsilyloxy-propyl(ethyl)phosphinate as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05013863
Source datasetuspto-grants-1991_05
ORD IDord-34d06ccad4fa445ea625a5044d428ea3
Source noteuspto-grants-1991_05