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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11988Generated: October 25, 2026

6-Bromo-2-naphthalenol → 6-Bromo-1-chloronaphthalen-2-ol

https://huagongshe.com/reaction/11988

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-2-naphthalenolHCID 27144—
ReactantChlorosuccinimideHCID 31398—
CatalystZirconium chloride (ZrCl4), (T-4)-HCID 9856075—
SolventDichloromethaneHCID 6344—
Product6-Bromo-1-chloronaphthalen-2-olHCID 2204815995.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

The synthesis of (S1-2) was carried out following the method described in Synlett, No. 18, 2837 (2005), wherein 29.9 g of N-chlorosuccinimide and 600 ml of dichloromethane were added to a reactor in nitrogen atmosphere and cooled to 0° C., 2.6 g of zirconium (IV) chloride was added, and then 50 g of 6-bromo-2-naphthol (S1-1) was added slowly. The reaction solution was heated to room temperature and stirred for 10 hours, then washed with saturated sodium bicarbonate solution and water, dried over magnesium sulfate, and distilled under a reduced pressure to remove the solvent. Recrystallization was carried out using a mixed solvent of toluene/heptane=1/1 (volumetric ratio) to obtain 55 g of 6-bromo-1-chloro-2-naphthol (S1-2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727417B2
Source datasetuspto-grants-2010_06
ORD IDord-8195caeae8504cdfb40a16fc4ca39ca5
Source noteuspto-grants-2010_06