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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771479Generated: November 2, 2026

6-Bromo-2-naphthalenol → 6-Bromo-1-fluoronaphthalen-2-OL

https://huagongshe.com/reaction/1771479

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-2-naphthalenolHCID 27144—
ReactantSelectfluorHCID 2724933—
SolventAcetonitrileHCID 6342—
Product6-Bromo-1-fluoronaphthalen-2-OLHCID 1124194083%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 6-bromonaphthalen-2-ol (2.23 g, 10.0 mmol) in CH3CN (50 mL) was added Selectfluor (4.20 g, 12.0 mmol). The reaction mixture was heated at 60° C. overnight and concentrated. The residue was partitioned between water (50 mL) and EtOAc (100 mL). The aqueous phase was separated and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel chromatography to give 6-bromo-1-fluoronaphthalen-2-ol using ethyl acetate and hexanes as solvents (2.0 g, 83% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249132B2
Source datasetuspto-grants-2016_02
ORD IDord-115a6403f829427e915e8596b90714cd
Source noteuspto-grants-2016_02