HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901756Generated: October 30, 2026
Dimethyl Sulfoxide → 1-(2,2-Diphenylvinyl)-3,5-dibromobenzene
https://huagongshe.com/reaction/901756
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | 3,5-Dibromobenzaldehyde | HCID 622077 | — |
| Reactant | Diethyl benzhydrylphosphonate | HCID 10267017 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(2,2-Diphenylvinyl)-3,5-dibromobenzene | HCID 22138031 | 74% |
Reaction Steps
Under an atmosphere of argon, 3,5-dibromobenzaldehyde (12.1 g, 46 mmole) and diethyl diphenylmethylphosphonate (15 g, 49 mmole, 1.1 eq) were dissolved into dimethyl sulfoxide (DMSO) (60 ml). To the resultant solution, potassium t-butoxide (6.2 g, 55 mmole, 1.2 eq) was added in small portions and the obtained solution was stirred at the room temperature for 9 hours and left standing for one night. After water (60 ml) was added, the reaction mixture was subjected to extraction with ethyl acetate (250 ml). The obtained organic layer was washed with water (100 ml) and a saturated aqueous solution of sodium chloride (50 ml) and dried with magnesium sulfate. Then, the solvent was removed by distillation and a deep brown oil was obtained. The obtained oil was purified by the column chromatography (silica gel/hexane and hexane+3% dichloromethane, successively) and a white solid (14.0 g, 74%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07361796B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-7bb6aef65834474daca6eca4c6bfc21a |
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| Source note | uspto-grants-2008_04 |
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