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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427608Generated: October 25, 2026

Benzyl Bromide → 2-Benzyloxy-1-methyl-4-nitro-benzene

https://huagongshe.com/reaction/427608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium CarbonateHCID 10340—
Reactant2-Methyl-5-nitrophenolHCID 93576—
SolventAcetoneHCID 180—
Product2-Benzyloxy-1-methyl-4-nitro-benzeneHCID 1817450233.5%

Reaction Steps

To a stirred suspension of 2-methyl-5-nitrophenol (2.0 g, 13 mmol) and sodium carbonate (1.94 g, 18.3 mmol) in acetone was added benzyl bromide (1.7 mL, 14 mmol). The mixture was heated to reflux for 24 h, cooled, filtered, and the solid washed with acetone. The filtrate and acetone washings were combined and concentrated in vacuo. Recrystallization from ether/hexanes gave 1.06 g (33%) of the title product as an off-white solid. MS-FD 243 m/e (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313122B1
Source datasetuspto-grants-2001_11
ORD IDord-975c64ed7ad244fab979da9af431510a
Source noteuspto-grants-2001_11