HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892476Generated: October 28, 2026
Hexane → 4-(Bromomethyl)-2-fluorobenzoic acid
https://huagongshe.com/reaction/1892476
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Fluoro-4-methylbenzoic acid | HCID 2736145 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(Bromomethyl)-2-fluorobenzoic acid | HCID 18510270 | 53.9% |
Reaction Steps
To a solution of 2-fluoro-4-methylbenzoic acid (1.029 g, 6.678 mmol) in carbon tetrachloride (10 ml) were added N-bromosuccinimide (1.189 g, 6.682 mmol) and 2,2′-azobisisobutyronitrile (43.9 mg, 0.267 mmol). After stirring at 90° C. for 30 min and at 100° C. for 2.5 hr, the mixture was cooled to 0° C. The precipitate was collected by filtration and washed with hexane and water to give a crude product. The crude product was dissolved in ethyl acetate (5 ml), and hexane (10 ml) was added. The precipitated solid was collected by filtration, and dried under reduced pressure to give 4-(bromomethyl)-2-fluorobenzoic acid (838.6 mg, 3.599 mmol, yield 53.9%) as a slightly yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507690B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-36c165751c56437fbd303adda537f4b5 |
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| Source note | uspto-grants-2013_08 |
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