Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDiethyl benzylphosphonateHCID 14122—
ReactantHCID 22138045HCID 22138045—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
Product9-Bromo-10-(4-(2-phenylvinyl)phenyl)anthraceneHCID 7386685286%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053255B2
Source datasetuspto-grants-2006_05
ORD IDord-0651a1819aef488eadbe124b08eb7a28
Source noteuspto-grants-2006_05