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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892476Generated: October 28, 2026

Hexane → 4-(Bromomethyl)-2-fluorobenzoic acid

https://huagongshe.com/reaction/1892476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Fluoro-4-methylbenzoic acidHCID 2736145—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
SolventEthyl AcetateHCID 8857—
Product4-(Bromomethyl)-2-fluorobenzoic acidHCID 1851027053.9%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507690B2
Source datasetuspto-grants-2013_08
ORD IDord-36c165751c56437fbd303adda537f4b5
Source noteuspto-grants-2013_08