HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827624Generated: October 25, 2026
Dimethyl Sulfoxide → 9-Bromo-10-(4-(2-phenylvinyl)phenyl)anthracene
https://huagongshe.com/reaction/1827624
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diethyl benzylphosphonate | HCID 14122 | — |
| Reactant | HCID 22138045 | HCID 22138045 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Product | 9-Bromo-10-(4-(2-phenylvinyl)phenyl)anthracene | HCID 73866852 | 86% |
Reaction Steps
Under an atmosphere of argon, 9-bromo-10-(4-formylphenyl)anthracene (3.9 g, 11 mmole) and diethyl benzylphosphonate (3 g, 13 mmole, 1.2 eq) were suspended into DMSO (25 ml). To the resultant suspension, potassium t-butoxide (1.6 g, 14 mmole, 1.1 eq) was added and the obtained mixture was stirred at the room temperature for 10 hours and left standing for one night. The reaction mixture was diluted with water (50 ml) and subjected to extraction with toluene (300 ml). The organic layer was washed with water (50 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 yellow solid was obtained. The obtained solid was purified by recrystallization from toluene (40 ml) and yellow needle crystals (4.1 g, 86%) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07053255B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-0651a1819aef488eadbe124b08eb7a28 |
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| Source note | uspto-grants-2006_05 |
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