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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721350Generated: October 31, 2026

Benzyl Bromide → HCID 22414647, compound

https://huagongshe.com/reaction/1721350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-5-methyl-4-nitrophenolHCID 22414640—
SolventAcetoneHCID 180—
ProductHCID 22414647HCID 22414647—

Reaction Steps

To a solution of 85.6 g 2-nitro-4-fluoro-5-hydroxy-toluene (0.5 mol) in 1300 ml acetone are added at room temperature 138 g K2CO3 (1.0 mol). 72 ml benzyl bromide (0.6 mol) are then added dropwise over 1 hour and the resulting mixture is stirred overnight at 60°. The solvent is evaporated and the residue taken up in AcOEt. The precipitate is removed by filtration and the solution is washed with water. The organic layer is dried over sodium sulfate, the solvent evaporated and the residue crystallized from hexane to yield 2-nitro-4-fluoro-5-benzyloxy-toluene. M.p.=95°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05510353
Source datasetuspto-grants-1996_04
ORD IDord-2fae6b87a5294ad89036787d4e4ea2d1
Source noteuspto-grants-1996_04