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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644214Generated: November 1, 2026

1-Naphthol → 4-Bromonaphthalen-1-ol

https://huagongshe.com/reaction/1644214

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphtholHCID 7005—
ReactantN-bromobutanimideHCID 67184—
SolventAcetonitrileHCID 6342—
Product4-Bromonaphthalen-1-olHCID 57560964%

Reaction Steps

To a solution of naphthol (12, 5.0 g, 35 mmol) in CH3CN (125 mL) at 0° C. was added N-bromosuccinimide (7.9 g, 45 mmole) in several portions. The reaction mixture was warmed to room temperature, stirred for 1 h, and concentrated. The residue was dissolved in EtOAc (500 mL) and the solution was washed with water (300 mL) and brine (300 mL). The organic layer was dried over MgSO4, filtered, and concentrated. The residue was purified by column chromatography (silica gel, 4:1 hexanes/EtOAc) to afford 4-bromonaphthol (13, 5.0 g, 64%) as a white solid: 1H NMR (300 MHz, CDCl3) δ 8.22-8.16 (m, 2H), 7.62-7.26 (m, 3H), 6.71 (d, J=8.0 Hz, 1H), 5.46 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124607B2
Source datasetuspto-grants-2012_02
ORD IDord-3e50b182f21b4a688e5b4c737faa7dc3
Source noteuspto-grants-2012_02