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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288907Generated: October 30, 2026

Hydrogen Bromide → 1-Hydroxy-5-phenoxynaphthalene

https://huagongshe.com/reaction/2288907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant1-Methoxy-5-phenoxynaphthaleneHCID 18702041—
SolventAcetic AcidHCID 176—
Product1-Hydroxy-5-phenoxynaphthaleneHCID 1870204060.1%

Reaction Conditions

Temperature97.5 °C

Reaction Steps

Into 50 mL of glacial acetic acid, 3.7 g of 1-methoxy-5-phenoxynaphthalene prepared as above, followed by 20 mL of 40% aqueous hydrogen bromide was stirred. The mixture was heated at 95-100° C. for 16 hours. The solvent was removed under vacuum, and the residue was redissolved in ethyl acetate and washed three times with brine. The organic layer was dried over magnesium sulfate and filtered. After removing solvent, the residue was chromatographed over silica gel with a gradient elution of 0 to 30% ethyl acetate in hexane, providing 2.10 g (59%) of 1-hydroxy-5-phenoxynaphthalene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090850
Source datasetuspto-grants-2000_07
ORD IDord-d1b49b4548f74fc59f1de55bc3c97665
Source noteuspto-grants-2000_07