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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725079Generated: November 2, 2026

N-bromobutanimide → 4-Bromo-2-(bromomethyl)-1-fluorobenzene

https://huagongshe.com/reaction/1725079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-Bromo-2-fluorotolueneHCID 123527—
SolventCarbon TetrachlorideHCID 5943—
Product4-Bromo-2-(bromomethyl)-1-fluorobenzeneHCID 13553295—

Reaction Steps

To a solution of 5-bromo-2-fluorotoluene (15 g, 0.079 mole) in CCl4 (150 mL) was added NBS (14.2 g, 0.080 mole). The resulting reaction solution was heated under reflux with the starting material being completely consumed within 2 hr. CCl4 was removed under reduced pressure and the residue was diluted, dissolved in ether, washed with brine (3×), dried over MgSO4, and concentrated. Chromotography in hexane yielded 5-bromo-2-fluorobenzyl bromide. The product was immediately used for the reaction below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488822B2
Source datasetuspto-grants-2009_02
ORD IDord-5a258718c4034e13b2a035a9f7c0db6f
Source noteuspto-grants-2009_02