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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778754Generated: October 31, 2026

N-bromobutanimide → Benzoic acid, 4-bromo-2-(bromomethyl)-5-fluoro-, methyl ester

https://huagongshe.com/reaction/1778754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 4-bromo-5-fluoro-2-methylbenzoateHCID 56965486—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
ProductBenzoic acid, 4-bromo-2-(bromomethyl)-5-fluoro-, methyl esterHCID 8672285192%

Reaction Steps

A mixture of methyl 4-bromo-5-fluoro-2-methylbenzoate (1.0 g, 4.0 mmol) (Ellanoval Laboratories Cat. No. 38-0304), N-bromosuccinimide (900. mg, 5.06 mmol) and benzoyl peroxide (50 mg, 0.2 mmol) in carbon tetrachloride (50 mL) was refluxed under a nitrogen atmosphere for 4 h. After cooling the mixture was diluted with methylene chloride. The organic solution was washed with brine, then dried over Na2SO4. After filtration the filtrate was concentrated under reduced pressure. The residue was purified by flash chromatography on a silica gel column with ethyl acetate in hexanes (0-50%) to afford the desired product (1.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266892B2
Source datasetuspto-grants-2016_02
ORD IDord-86fab34a200342bca443c837844284fe
Source noteuspto-grants-2016_02