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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193484Generated: October 25, 2026

Benzyl Bromide → 1-Benzyloxy-3-methyl-2-nitrobenzene

https://huagongshe.com/reaction/1193484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Methyl-2-nitrophenolHCID 21026—
SolventDimethylformamideHCID 6228—
Product1-Benzyloxy-3-methyl-2-nitrobenzeneHCID 334418788.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 3-methyl-2-nitrophenol (50 g, 0.326 mol), K2CO3 (45 g, 0.326 mol) and benzylbromide (61.4 g, 42.6 mL, 0.359 mol) in dry DMF (200 mL) was stirred at 90° C. for 3 hours under nitrogen. Most of the DMF was removed at reduced pressure and the residue was partitioned between water (300 mL) and ether (300 mL). The organic layer was washed with brine and dried (Na2SO4). Removal of the solvent provided (70 g, 88%) of 3-benzyloxy-2-nitrotoluene as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04810699
Source datasetuspto-grants-1989_03
ORD IDord-a704537da871413fb26b32dab55ba06d
Source noteuspto-grants-1989_03