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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660826Generated: November 1, 2026

Benzyl Bromide → 2-(Benzyloxy)-4-fluoro-1-nitrobenzene

https://huagongshe.com/reaction/660826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant5-Fluoro-2-nitrophenolHCID 9937—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product2-(Benzyloxy)-4-fluoro-1-nitrobenzeneHCID 11096908—

Reaction Steps

To a stirred solution of 5-fluoro-2-nitrophenol (1.57 g, 10 mmol) and benzyl bromide (1.25 mL, 10.5 mmol) in DMF (20 mL) is added K2CO3 (2.07 g, 15 mmol) and the suspension is stirred at RT overnight. The reaction is quenched with water and the aqueous layer is extracted with EtOAc. The combined organic layers are washed with water and brine, then dried over MgSO4 and filtered. The solvent is removed under reduced pressure to give the product as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084448B2
Source datasetuspto-grants-2011_12
ORD IDord-08a3af75e94b4a6dbf2045662035e984
Source noteuspto-grants-2011_12