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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400314Generated: November 2, 2026

Hydrogen Bromide → 6-Bromo-1-chloronaphthalen-2-ol

https://huagongshe.com/reaction/1400314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant1-Chloro-2-naphtholHCID 12459—
SolventHydrogen PeroxideHCID 784—
SolventMethanolHCID 887—
Product6-Bromo-1-chloronaphthalen-2-olHCID 22048159—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 400 mg (2.24 mmol) of 1-chloronaphthalen-2-ol in 3 mL of MeOH, HBr (purum p.a., ≧62%, 270 μL) and H2O2 (50 wt. % in water solution, 27 μL) were added. The resulting mixture was heated at 40° C. and stirred overnight. The mixture was quenched with water (10 mL) and extracted with ethyl acetate (10 mL×2). The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to afford 6-bromo-1-chloronaphthalen-2-ol as pale yellow solid which was used in the next step without further purification. HPLC-MS (ESI+): m/z 258.51 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906946B2
Source datasetuspto-grants-2014_12
ORD IDord-9078dd4278fc4761b10edbc740a437f8
Source noteuspto-grants-2014_12