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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640006Generated: November 2, 2026

Benzoyl Peroxide → Ethyl 2-(bromomethyl)-5-chlorobenzoate

https://huagongshe.com/reaction/1640006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 5-chloro-2-methylbenzoateHCID 21269135—
Solvent1,2-DichloroethaneHCID 11—
ProductEthyl 2-(bromomethyl)-5-chlorobenzoateHCID 1327246369.2%

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of ethyl 5-chloro-2-methylbenzoate (3.20 g, 16.1 mmol), N-bromosuccinimide (3.15 g, 17.7 mmol) and benzoyl peroxide (0.39 g, 1.61 mmol) in 1,2-dichloroethane (90 mL) was heated to 75° C. in an oil bath for 4 h. After this time, the mixture was cooled to room temperature and the organic layer was washed with water (45 mL) and brine (45 mL). The organic layer was then dried over magnesium sulfate and concentrated under reduced pressure. Purification by flash chromatography (silica, 1:20 ethyl acetate/hexanes) afforded ethyl 2-(bromomethyl)-5-chlorobenzoate (3.09 g, 68%) as a clear oil: 1H NMR (500 MHz, CDC13) 7.94 (d, J=2.5 Hz, 1H), 7.46 (dd, J=8.5, 2.5 Hz, 1H), 7.40 (d, J=8.0 Hz, 1H), 4.91 (s, 2H), 4.42 (q, J=7.0 Hz, 2H), 1.43 (t, J=7.0 Hz, 3H); ESI MS m/z 279 [(M+2)+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110681B2
Source datasetuspto-grants-2012_02
ORD IDord-df0590a0be1340c3a625f52c44e55cf8
Source noteuspto-grants-2012_02