Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820697Generated: October 29, 2026

Water → 1-Bromo-3-(4-methoxybenzyloxy)-2-methylbenzene

https://huagongshe.com/reaction/1820697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Methoxybenzyl alcoholHCID 7738—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-6-fluorotolueneHCID 2736335—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventHeptaneHCID 8900—
SolventSodium chloride; waterHCID 57417360—
Product1-Bromo-3-(4-methoxybenzyloxy)-2-methylbenzeneHCID 6688185546%

Reaction Steps

1-Bromo-3-fluoro-2-methylbenzene (388 mg, 2.05 mmol), and (4-methoxyphenyl)methanol (0.511 mL, 4 mmol) were dissolved in DMF (5 mL) in a microwave vessel. Sodium hydride as a 60% dispersion in mineral oil (164 mg, 4.0 mmol) was added portionwise under a flow of nitrogen over 10 min. The reaction vessel was then sealed and heated at 180° C. for 900s. The crude reaction mixture was poured onto 1:1 water:brine (6 mL) and DCM (10 mL). The biphasic mixture was stirred at ambient temperature for 1 h and then the organic and aqueous layers were separated. The combined organics were dried over Na2SO4 and concentrated in vacuo. The crude material was then purified by chromatography on silica gel. Elution with 5:95 ethyl acetate:heptane afforded 1-bromo-3-(4-methoxybenzyloxy)-2-methylbenzene (289 mg, 0.9 mmol, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605170B2
Source datasetuspto-grants-2009_10
ORD IDord-dc8c987f83e246a5a1e324424767899d
Source noteuspto-grants-2009_10