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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411932Generated: October 30, 2026

Methyltriphenylphosphonium iodide → 3,5-Bis(3',5'-di-t-butylstyryl)styrene

https://huagongshe.com/reaction/411932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyltriphenylphosphonium iodideHCID 638159—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant3,5-Bis[2-(3,5-di-tert-butylphenyl)ethenyl]benzaldehydeHCID 54028687—
SolventTetrahydrofuranHCID 8028—
Product3,5-Bis(3',5'-di-t-butylstyryl)styreneHCID 5385170695%

Reaction Steps

Dry tetrahydrofuran (375 mL) was added to a mixture of methyltriphenylphosphonium iodide (50.6 g, 125 mmoles) and potassium t-butoxide (14.0 g, 125 mmoles) and stirred at room temperature for 15 minutes. 3,5-bis(3′,5′-di-t-butylstyryl)benzaldehyde (44.6 g, 83.4 mmoles) was then added and the reaction mixture was stirred at room temperature for 90 minutes. The solvent was then evaporated and the remaining sludge was triturated with dichloromethane-pet.ether (40-60) (1:9) and filtered through silica, rinsing thoroughly with the same solvent mixture. The crude product was recrystallised from dichloromethane/methanol to give white crystals of 3,5-bis(3′,5′-di-t-butylstyryl)styrene (42.15 g, 95%) m.p. 143-145° C. with microanalysis i/r, u/v, NMR and mass spectrographic data substantially identical to that of the first example.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06558818B1
Source datasetuspto-grants-2003_05
ORD IDord-4860cb35bd794a1491f259d2134c0638
Source noteuspto-grants-2003_05