HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571805Generated: October 31, 2026
Hydrochloric Acid → 1-(4-Bromo-3-fluorophenyl)-2-chloroethan-1-one
https://huagongshe.com/reaction/571805
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 4-Bromo-3-fluorobenzoyl chloride | HCID 22626891 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Bromo-3-fluorophenyl)-2-chloroethan-1-one | HCID 53350328 | — |
Reaction Steps
To a stirred solution of 4-bromo-3-fluorobenzoyl chloride (5.6 g, CAS 695188-21-7) in acetonitrile (30 ml) and THF (30 ml) at 0-5° C. was added dropwise (trimethylsilyl)diazomethane (13.7 ml, 2 M solution in diethyl ether). The reaction mixture was stirred at room temperature for 30 min TLC analysis showed the reaction was complete. Hydrochloric acid (3.81 ml, 37% aq.) was then added dropwise at 0-5° C. over 10 minutes and the reaction mixture was then stirred at room temperature for a further 20 minutes. The reaction mixture was poured into EtOAc and extracted sequentially with aq. Na2CO3 solution, water and saturated brine. The organic layer was then dried over Na2SO4 and concentrated in vacuo to afford 2-chloro-1-(4-bromo-3-fluoro-phenyl)-ethanone (5.67 g) as a yellow solid which was used in the next step without further purification. MS (EI): 203 ([{81Br}M-CH2Cl]+), 201 ([{79Br}M-CH2Cl]+), 175 ([{81Br}M-CH2Cl—CO]+), 173 ([{79Br}M-CH2Cl—CO]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029370B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-720a69f1cfd34442af2331b80ca307e8 |
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| Source note | uspto-grants-2015_05 |
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