HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66046Generated: October 28, 2026
Water → Bis(chloromethyl)(oxo)phenyl-lambda~5~-phosphane
https://huagongshe.com/reaction/66046
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Phosphinic chloride, bis(chloromethyl)- | HCID 139476 | — |
| Reactant | HCID 178478979 | HCID 178478979 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Bis(chloromethyl)(oxo)phenyl-lambda~5~-phosphane | HCID 12600705 | — |
Reaction Steps
A three-necked reaction vessel equipped with a reflux condenser, mechanically driven stirrer, nitrogen inlet and thermometer was charged with 91 g. of bis(chloromethyl)phosphinic chloride and 150 cc. tetrahydrofuran. A 280 g. portion of a tetrahydrofuran solution containing 2.0 moles of phenylmagnesium chloride per kilogram of solution was gradually added to the reaction mixture at a rate such that the temperature of the reaction mixture did not exceed 30° C. The resultant mixture was stirred for one hour following completion of the addition, at which time an excess of water was added and the organic phase isolated. The aqueous phase was extracted once with chloroform and the chloroform layer combined with the previously isolated organic layer. The organic solvents were then evaporated under reduced pressure to yield an offwhite solid which was slurried with a small amount of diethyl ether and filtered. The isolated solid material weighed 62.0 g. and melted from 135° to 137° C. The reported melting range for the compound is 141°-142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04130411 |
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| Source dataset | uspto-grants-1978_12 |
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| ORD ID | ord-ac5657ef6ba24bf1a1698e96295549e3 |
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| Source note | uspto-grants-1978_12 |
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