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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643352Generated: October 31, 2026

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

https://huagongshe.com/reaction/1643352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantBenzene, 1-bromo-3,5-dimethyl-HCID 136357—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
SolventHexaneHCID 8058—
Product1-Bromo-3-(bromomethyl)-5-methylbenzeneHCID 2232426194.2%

Reaction Steps

A mixture of 3,5-dimethylbromobenzene (70 g, 0.378 M), NBS (67.3 g, 0.373 M), and benzoyl peroxide (2.27 g, 0.009 M) in carbon tetrachloride (300 mL) was refluxed for 3 hr. After cooling to room temperature, the mixture was filtered and the filtrate was evaporated in vacuo to give a pale brown oil. The crude product was dissolved in hexane and filtered through a short silica gel pad (diameter: 9.5 cm, height: 7 cm). The silica gel pad was washed with hexane until the product eluted completely. The filtrate was evaporated in vacuo to give 94 g of 1-bromo-3-(bromomethyl)-5-methylbenzene (contaminated with starting material and 1-bromo-3,5-bis-bromomethylbenzene) as a pale brown oil, which solidified on standing at room temperature. The mixture was used directly in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119800B2
Source datasetuspto-grants-2012_02
ORD IDord-d89c5f57c1684aa5b7c64b5fc0d5f365
Source noteuspto-grants-2012_02