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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912154Generated: November 1, 2026

Sulfuric Acid → Phosphine, tricyclopentyl-

https://huagongshe.com/reaction/1912154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTolueneHCID 1140—
ReactantPhosphorus trichlorideHCID 24387—
ReactantChlorocyclopentaneHCID 70252—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178478989HCID 178478989—
SolventTetrahydrofuranHCID 8028—
ProductPhosphine, tricyclopentyl-HCID 4463278—

Reaction Conditions

Temperature25 °C

Reaction Steps

A 200-ml four-necked flask sufficiently purged with nitrogen was equipped with a stirrer, a thermometer and a reflux condenser. 5.5 g (40 mmol) of trichlorophosphine and 40.0 ml of tetrahydrofuran were weighed in the flask. A cyclopentylmagnesium chloride solution was added dropwise to the flask at an internal temperature of 10-20° C. over a period of 3 hours, wherein the solution had been previously prepared from 13.8 g (132 mmol) of cyclopentyl chloride and 3.2 g (132 mmol) of metallic magnesium in 49 g of tetrahydrofuran. The mixture was stirred at 20-30° C. for 2 hours. Gas chromatography analysis confirmed the disappearance of trichlorophosphine. After the completion of the reaction, 61 ml of toluene was added, and 11.8 g (6 mmol) of 5% sulfuric acid was added dropwise to dissolve the magnesium salt, followed by separation. The organic phase was washed with 11.8 ml of water, and a solution of tricyclopentylphosphine was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604249B2
Source datasetuspto-grants-2013_12
ORD IDord-728bb12f001b46dca8d24cc2a1328e57
Source noteuspto-grants-2013_12