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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337619Generated: October 30, 2026

Benzoyl Peroxide → 2-(Bromomethyl)-1-chloro-4-(2-methoxyethoxy)benzene

https://huagongshe.com/reaction/337619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 22467254HCID 22467254—
SolventCarbon TetrachlorideHCID 5943—
Product2-(Bromomethyl)-1-chloro-4-(2-methoxyethoxy)benzeneHCID 59177555—

Reaction Steps

A mixture of 1-chloro-4-(2-methoxyethoxy)-2-methylbenzene (1 eq.) from the previous step, NBS (1.1 eq.) and benzoyl peroxide (0.05 eq.) in CCl4 (0.2 M) was refluxed for 2 h. The volatiles were then removed in vacuo and the resulting residue was suspended in hexanes. The insolubles were removed via filtration and washed further with hexanes. The filtrate was concentrated in vacuo to afford the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889714B2
Source datasetuspto-grants-2014_11
ORD IDord-34047ed8e1f54db7a6d2fbe6d7aa3373
Source noteuspto-grants-2014_11