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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634997Generated: October 31, 2026

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

https://huagongshe.com/reaction/1634997

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 numberUS06509334B1
Source datasetuspto-grants-2003_01
ORD IDord-67686e349bf1421ca3d11186a27d7552
Source noteuspto-grants-2003_01