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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576927Generated: October 25, 2026

Benzoyl Peroxide → 2-(Bromomethyl)-1-chloro-4-methoxybenzene

https://huagongshe.com/reaction/576927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant1-Chloro-4-methoxy-2-methylbenzeneHCID 458156—
SolventCarbon TetrachlorideHCID 5943—
Product2-(Bromomethyl)-1-chloro-4-methoxybenzeneHCID 12484533—

Reaction Steps

To a solution of the 1-chloro-4-methoxy-2-methylbenzene (2.0 g, 12.77 mmol) in anhydrous carbon tetrachloride (50 mL), NBS (2.29 g, 12.98 mmol) and benzoyl peroxide (0.154 g, 0.64 mmol) was added. The reaction mixture was heated to reflux overnight. Then, the reaction mixture was cooled to room temperature and filtered. The filtrate was evaporated to provide crude 2-(bromomethyl)-1-chloro-4-methoxybenzene, which was used for the next step without any further purification; 1H NMR (400 MHz, DMSO-d6): δ 3.74 (s, 3H), 4.66 (s, 2H), 7.01 (d, J=8.9 Hz, 1H), 7.19 (s, 1H), 7.38 (d, J=8.9 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040538B2
Source datasetuspto-grants-2015_05
ORD IDord-2da1d7db5d564acf8b4fc88aa3599a3e
Source noteuspto-grants-2015_05