HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436412Generated: November 3, 2026
Hexane → 2-Bromo-1-(4-bromo-2-fluorophenyl)ethanone
https://huagongshe.com/reaction/1436412
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-(4-Bromo-2-fluorophenyl)ethan-1-one | HCID 21938581 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-1-(4-bromo-2-fluorophenyl)ethanone | HCID 22121483 | 97% |
Reaction Steps
Bromine (1.2 mL, 23.0 mmol) in 10 mL of glacial acetic acid was added drop-wise to a solution of 1-(4-bromo-2-fluoro-phenyl)-ethanone (5.0 g, 23.0 mmol), prepared in the previous step, in 150 mL of dry methylene chloride at 0° C. After the addition, the reaction was allowed to warm to room temperature. TLC (5% ethyl acetate:hexane) indicated the starting material was consumed. The reaction was diluted with methylene chloride and washed with 5% sodium thiosulfate and brine. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 2-bromo-1-(4-bromo-2-fluoro-phenyl)-ethanone (6.6 g, 97%) as a light green oil. This compound was used without further purification. MS (ES) m/z 297 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07618990B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-f19e8f0b3ac4465a9ce0100b1bdd1b5b |
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| Source note | uspto-grants-2009_11 |
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