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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536570Generated: October 27, 2026

Benzyl Bromide → (2-(Benzyloxy)-5-bromophenyl)methanol

https://huagongshe.com/reaction/536570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium HydroxideHCID 14798—
Reactant5-Bromo-2-hydroxybenzyl alcoholHCID 75342—
SolventEthanolHCID 702—
Product(2-(Benzyloxy)-5-bromophenyl)methanolHCID 89713682.1%

Reaction Steps

A solution of 5-bromo-2-hydroxybenzylalcohol (3.677 g, 18.11 mmol) in abs. EtOH (80 ml) and NaOH (0.797 g, 19.921 mmol) was stirred under a N2 atmosphere for 20 min at RT then a solution of benzylbromide (2.15 ml, 18.11 mmol) in abs. EtOH (10 ml) was added and the mixture was stirred at RT overnight. The volatiles was removed under vacuum. The reminder was partitioned between HCl (2M aq.) and EtOAc. The organic layer was washed with brine, dried (MgSO4) and evaporated to dryness. The residue was purified by MPLC (50 g SiO2 cartridge, eluent 90% iso-hexane-10% EtOAc) yielding 4.36 g of (2-benzyloxy-5-bromo-phenyl)-methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859606B2
Source datasetuspto-grants-2014_10
ORD IDord-fdeb12b724ac4df7874bda2fa5aabaad
Source noteuspto-grants-2014_10