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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085891Generated: October 31, 2026

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

https://huagongshe.com/reaction/2085891

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 numberUS06720093B2
Source datasetuspto-grants-2004_04
ORD IDord-a9d85e97c851424d873731c8df8200f0
Source noteuspto-grants-2004_04