HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979712Generated: October 27, 2026
Water → Cyclohexylisopropylphenylphosphine
https://huagongshe.com/reaction/979712
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Phenyl phosphorus dichloride | HCID 12573 | — |
| Reactant | HCID 178418365 | HCID 178418365 | — |
| Reactant | HCID 178478990 | HCID 178478990 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Cyclohexylisopropylphenylphosphine | HCID 54482329 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04668823 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-1bc44ea8ae3b489d992bbdb64b47c907 |
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| Source note | uspto-grants-1987_05 |
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