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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426179Generated: October 25, 2026

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

https://huagongshe.com/reaction/426179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantBenzene, 1-bromo-3,5-dimethyl-HCID 136357—
CatalystBenzoyl PeroxideHCID 7187—
CatalystTungstenHCID 23964—
SolventCarbon TetrachlorideHCID 5943—
Product1-Bromo-3-(bromomethyl)-5-methylbenzeneHCID 2232426172%

Reaction Steps

A mixture of 3,5-dimethylbromobenzene (80.25 g, 0.43M), NBS (77 g, 0.43M), and benzoyl peroxide (5.2 g, 0.021M) in carbon tetrachloride (400 ml) was refluxed for 3 hr. under a light of 500 W tungsten light. After cooling to room temperature, the mixture was filtered and the filtrate was evaporated in vacuo to give a white solid, which was purified by silica gel column chromatography (eluent, hexane) to afford 82 g (72%) of a white solid. m.p. 46-47° C.; 1H NMR (200 MHz, CDCl3) δ 2.32 (3H, s), 4.38 (2H, s), 7.12 (1H, s), 7.25 (1H, s), 7.33 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106064B2
Source datasetuspto-grants-2012_01
ORD IDord-c4a5f67c3a984322b10671c0051ad614
Source noteuspto-grants-2012_01