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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210781Generated: November 1, 2026

Chlorotrimethylsilane → ethyl P-(3-cyano-1,1,1-trifluoro-prop-2-yl)-P-methyl-phosphinate

https://huagongshe.com/reaction/2210781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
Reactant4,4,4-trifluorocrotononitrileHCID 5708782—
ReactantO-ethyl-P-methyl-phosphonous acidHCID 13145048—
SolventTetrahydrofuranHCID 8028—
Productethyl P-(3-cyano-1,1,1-trifluoro-prop-2-yl)-P-methyl-phosphinateHCID 10421332—

Reaction Steps

A solution of 2.16 g (20 mmol) of O-ethyl-P-methyl-phosphonous acid and 4.05 g (40 mmol) of triethylamine in 100 ml of dry tetrahydrofuran is stirred under an atmosphere of argon at 25°. To this solution are added at 25° 4.35 g (40 mmol) of trimethylsilyl chloride over a period of 10 minutes. A white precipitate is formed. The reaction mixture is stirred at 25° for additional 16 hours. Then, 2.42 g (20 mmol) of 4,4,4-trifluorocrotononitrile, dissolved in 20 ml of dry tetrahydrofuran, are added at 25° over a period of 10 minutes. The reaction mixture is refluxed for 40 hours, cooled to 25°, poured into ice-water and extracted with dichloromethane. The extracts are combined, washed with water, dried over anhydrous sodium sulphate and evaporated under reduced pressure to dryness. The crude product is chromatographed on 200 g of silica gel with trichloromethane as eluent. The product-containing fractions are combined and evaporated to give ethyl P-(3-cyano-1,1,1-trifluoro-prop-2-yl)-P-methyl-phosphinate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05461040
Source datasetuspto-grants-1995_10
ORD IDord-7d31e164d63d44f6b66e9005163a7de3
Source noteuspto-grants-1995_10