Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | Chlorocyclopentane | HCID 70252 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178478989 | HCID 178478989 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Phosphine, tricyclopentyl- | HCID 4463278 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604249B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-728bb12f001b46dca8d24cc2a1328e57 |
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| Source note | uspto-grants-2013_12 |
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