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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510089Generated: November 2, 2026

2-Chloro-6-fluorobenzyl bromide → HCID 66920546, compound

https://huagongshe.com/reaction/1510089

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-fluorobenzyl bromideHCID 2773625—
ReactantHCID 45257316HCID 45257316—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66920546HCID 6692054634.6%

Reaction Steps

A solution of 500 mg (1.14 mmol) of the compound of example 16, step 1, in THF (8 ml) was cooled to −78° C. with an acetone/dry ice bath. Within 10 min a solution of n-butyllithium (0.55 ml, 1.36 mmol, 2.5 M in hexane) was added followed by 0.36 ml (2.27 mmol) of 2-chloro-6-fluoro-benzyl bromide. The cooling bath was removed and the reaction mixture was allowed to warm up slowly to room temperature and stirred overnight. The mixture was quenched with water and extracted with EA. The organic layer was separated, dried over sodium sulfate, filtered, and evaporated under reduced pressure. The residue was purified by preparative HPLC. The eluate was lyophilized overnight to give 216 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211885B2
Source datasetuspto-grants-2012_07
ORD IDord-4c6d6e091ed447a481f448852530ff3f
Source noteuspto-grants-2012_07