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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748867Generated: October 29, 2026

Benzyl Bromide → 2-Benzyloxy-1-bromo-6-methoxy-naphthalene

https://huagongshe.com/reaction/748867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-6-methoxynaphthalen-2-olHCID 18428746—
SolventDimethylformamideHCID 6228—
Product2-Benzyloxy-1-bromo-6-methoxy-naphthaleneHCID 1170290892.4%

Reaction Steps

Add 1-bromo-6-methoxy-naphthalen-2-ol (66.7 g, 264 mmol), potassium carbonate (K2CO3, 40.0 g, 290 mmol) and benzyl bromide (49.6 g, 290 mmol) to DMF (800 mL). Stir the mixture at ambient temperature for 1 hour. Add water (400 mL) to precipitate the product. Collect the precipitate and wash the filter cake with heptane (3×125 mL) then dry to provide 83.7 g of 2-benzyloxy-1-bromo-6-methoxy-naphthalene (86.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399867B2
Source datasetuspto-grants-2008_07
ORD IDord-8c5524639fee43bcad96b3b13764fd65
Source noteuspto-grants-2008_07