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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyltriphenylphosphonium iodide | HCID 638159 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 3,5-Bis[2-(3,5-di-tert-butylphenyl)ethenyl]benzaldehyde | HCID 54028687 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,5-Bis(3',5'-di-t-butylstyryl)styrene | HCID 53851706 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06720093B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-a9d85e97c851424d873731c8df8200f0 |
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| Source note | uspto-grants-2004_04 |
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