HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729214Generated: November 1, 2026
4-Bromostyrene → Diphenylphosphinostyrene
https://huagongshe.com/reaction/729214
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromostyrene | HCID 16263 | — |
| Reactant | Chlorodiphenylphosphine | HCID 66180 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | Buta-1,3-diynylbenzene | HCID 11355482 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diphenylphosphinostyrene | HCID 11437688 | — |
Reaction Steps
Polymerizable Gold Complex (3-1) was synthesized by reacting the gold complex obtained by the reaction between sodium tetrachloroaurate (III) and triphenylphosphine having a polymerizable functional group, with phenylbutadiyne synthesized by a known method (see, P. Cadiot and W. Chodkiewicz, Chemistry of Acetylenes, H. G. Viehe, ed., Marcel Dekker, New York (1969)). More specifically, 20 ml of dried THF was added to 341 mg (14 mmol) of magnesium and thereto, a 10 ml THF solution containing 2.70 g (15 mmol) of 4-bromostyrene was added dropwise to prepare a Grignard reagent. To the resulting solution, a 10 ml THF solution containing 2.50 g (11 mmol) of chlorodiphenylphosphine was added dropwise and stirred at room temperature of 1.5 hours. After removing the solvent by distillation under reduced pressure, the residue was purified by silica gel column chromatography and recrystallized from a hexane solution to obtain 2.30 g (8.3 mmol) of (4-vinylphenyl)diphenylphosphine Compound (B).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582363B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-223775f6a560431b879c384c695c6fee |
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| Source note | uspto-grants-2009_09 |
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