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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880431Generated: October 26, 2026

N-bromobutanimide → 5-Bromo-1-(bromomethyl)-2-fluoro-3-methylbenzene

https://huagongshe.com/reaction/1880431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-Bromo-2-fluoro-1,3-dimethylbenzeneHCID 2736298—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product5-Bromo-1-(bromomethyl)-2-fluoro-3-methylbenzeneHCID 66920654100.7%

Reaction Steps

To a stirred solution of 5-bromo-2-fluoro-1,3-dimethylbenzene (5.0 g, 25 mmol) in carbon tetrachloride (100.0 mL) was added N-bromosuccinimide (4.11 g, 23.1 mmol) and benzoyl peroxide (100.0 mg, 0.017 mmol). The reaction was heated at reflux for 7 hours. The reaction was filtered and the filtrate washed with 2N HCl, saturated aqueous sodium bicarbonate, water and brine. The organic phase was dried over sodium sulfate, filtered and concentrated. The residue was flash chromatographed (5% EtoAc/Haptanes) to obtain 6.56 g of 5-bromo-1-(bromomethyl)-2-fluoro-3-methylbenzene as an oil product. 1H NMR (400 MHz, CDCl3) δ ppm 2.22-2.36 (s, 3 H) 4.42 (d, J=0.98 Hz, 2 H) 7.21-7.37 (m, 2 H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318762B2
Source datasetuspto-grants-2012_11
ORD IDord-4b345bc30f60488db40c42acdba3cf03
Source noteuspto-grants-2012_11