HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436449Generated: October 25, 2026
Hexane → 2-Bromo-1-(4-chloro-3-fluorophenyl)ethanone
https://huagongshe.com/reaction/1436449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4'-Chloro-3'-fluoroacetophenone | HCID 3822077 | — |
| Reactant | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | 2-Bromo-1-(4-chloro-3-fluorophenyl)ethanone | HCID 23003295 | 69% |
Reaction Steps
To a solution of 1-(4-chloro-3-fluorophenyl)ethanone (3.4 g, 19.7 mmol), prepared in the previous step, in methylene chloride:methanol (1:3) was added tetrabutylammonium tribromide (9.5 g, 19.7 mmol) in portions. The reaction was monitored by TLC (3:1 hexane:ethyl acetate) until the starting material was consumed. The reaction solution was concentrated in vacuo and the residue was partitioned between diethyl ether and water. The layers were separated and the organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to give 4.2 g of crude product. The crude product was purified on silica gel using 5% ethyl acetate:hexane to give 2-bromo-1-(4-chloro-3-fluoro-phenyl)-ethanone (3.4 g, 69%) as desired product, MS (ES) m/z 252 [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-5080b2c6a2f24bc08863019aeb39f773 |
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| Source note | uspto-grants-2009_11 |
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