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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282465Generated: October 26, 2026

Triphenylethylene → 1-Bromo-1,2,2-triphenylethene

https://huagongshe.com/reaction/1282465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylethyleneHCID 6025—
ReactantBromineHCID 24408—
Solvent1,2-DichloroethaneHCID 11—
Product1-Bromo-1,2,2-triphenyletheneHCID 1535469.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a reactor were introduced 12.5 g (48.8 mmol) of the 1,1,2-triphenylethylene and 50 mL of 1,2-dichloroethane under a nitrogen atmosphere. The contents were cooled to 0° C., and 7.80 g (48.8 mmol) of bromine was gradually added dropwise thereto. This mixture was stirred at room temperature for 1 hour. The resultant reaction mixture was washed with saturated aqueous sodium hydrogen carbonate solution, saturated aqueous sodium thiosulfate solution, and saturated aqueous sodium chloride solution and then dried with anhydrous magnesium sulfate. Thereafter, the solvent was removed under reduced pressure. The resultant concentrate was recrystallized from ethanol and ethyl acetate to obtain 11.3 g (69%) of the target compound as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455720B1
Source datasetuspto-grants-2002_09
ORD IDord-cc48a919e86347428772c38c7d6007d9
Source noteuspto-grants-2002_09