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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667727Generated: November 1, 2026

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

https://huagongshe.com/reaction/1667727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluoro-4-nitrophenolHCID 520948—
SolventAcetonitrileHCID 6342—
Product4-Benzyloxy-2-fluoro-1-nitrobenzeneHCID 2218070496.3%

Reaction Steps

To a mixture of 3.14 g (20 mmole) of 3-fluoro-4-nitro-phenol, 100 mL of acetonitrile and 8.3 g (60 mmole) of potassium carbonate was added 2.5 mL (21 mmole) of benzyl bromide. The mixture was heated to reflux for 1 hour, then cooled and concentrated under reduced pressure. The residue was stirred with 100 mL for 30 minutes. The solid was collected by filtration and air dried to give 4.76 g of 4-benzyloxy-2-fluoro-1-nitro-benzene as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044213B2
Source datasetuspto-grants-2011_10
ORD IDord-762e32f5e2bf4205892689d251307d94
Source noteuspto-grants-2011_10