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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylethylene | HCID 6025 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 1-Bromo-1,2,2-triphenylethene | HCID 15354 | 69.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06455720B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-cc48a919e86347428772c38c7d6007d9 |
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| Source note | uspto-grants-2002_09 |
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