Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188953Generated: November 3, 2026

Benzyl Bromide → 1-Benzyloxy-2,3-difluoro-6-nitrobenzene

https://huagongshe.com/reaction/1188953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-Difluoro-6-nitrophenolHCID 2733745—
SolventDimethylformamideHCID 6228—
Product1-Benzyloxy-2,3-difluoro-6-nitrobenzeneHCID 1785888197%

Reaction Steps

A mixture of 2,3-difluoro-6-nitrophenol (15.1 g), benzyl bromide (10.8 mL) and potassium carbonate (11.9 g) in N,N-dimethylformamide (60 mL) was stirred at room temperature for 15 h. The reaction mixture was concentrated in vacuo and the residue was partitioned between ethyl acetate and water. The organic layer was washed with successively water and brine, dried (MgSO4), filtered, and concentrated to give the title compound (22.1 g, 97%) as a light yellow solid. MS 264 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673942B2
Source datasetuspto-grants-2014_03
ORD IDord-41e1ae67a5af4afab211cac53676dbb3
Source noteuspto-grants-2014_03