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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979712Generated: October 27, 2026

Water → Cyclohexylisopropylphenylphosphine

https://huagongshe.com/reaction/979712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenyl phosphorus dichlorideHCID 12573—
ReactantHCID 178418365HCID 178418365—
ReactantHCID 178478990HCID 178478990—
SolventDiethyl EtherHCID 3283—
ProductCyclohexylisopropylphenylphosphineHCID 5448232967%

Reaction Conditions

Temperature-25 °C

Reaction Steps

A Grignard mixture of 55 mmoles of cyclohexylmagnesium chloride (prepared from 1.5 g of magnesium turnings and 6.5 g of cyclohexylchloride in 20 ml of anhydrous ether) was added dropwise to a stirred solution of 8.9 g (50 mmoles) of phenyldichlorophosphine in 50 ml of anhydrous ether maintained under an inert atmosphere at -25° C. After the addition was complete, the resulting mixture was allowed to gradually warm to ambient temperature and then was refluxed for 15 minutes. The stirred mixture was cooled and a solution of 75 mmoles of isopropylmagnesium bromide (prepared from 2.1 g of magnesium turnings and 9.5 g of isopropyl bromide in 29 ml of anhydrous ether) was added dropwise at temperatures between 0° C. and +30° C. After refluxing for 4 hours, the reaction mixture was cooled to 0° C. and treated dropwise with 25 ml of water, thereby giving two phases. The ether phase was separated, dried over magnesium sulfate, concentrated, and distilled to give cyclohexylisopropylphenylphosphine: 31P-NMR δ=6.08 ppm; boiling point ("BP")=104°-105° C. at 0.05 torr, Chemical Ionization Mass Spec [M+H+ =235, yield=about 67%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04668823
Source datasetuspto-grants-1987_05
ORD IDord-1bc44ea8ae3b489d992bbdb64b47c907
Source noteuspto-grants-1987_05