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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166224Generated: November 4, 2026

Pyridine → 2-Bromo-4-chloro-6-nitrophenol

https://huagongshe.com/reaction/1166224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Chloro-2-nitrophenolHCID 6980—
ReactantBromineHCID 24408—
SolventDichloromethaneHCID 6344—
Product2-Bromo-4-chloro-6-nitrophenolHCID 29187182%

Reaction Steps

Bromine, Br2 (63.9 g) in 50 ml of dichloromethane was added dropwise to a solution of 4-chloro-6-nitrophenol (34.7 g) in 300 ml of dichloromethane. After the addition was completed, the mixture was stirred at room temperature for 30 min. Pyridine (19.0 g, 240 mmol) in 50 ml of dichloromethane was added. This mixture was stirred at room temperature for 2 hours and a white precipitate was formed. The reaction mixture was quenched with 200 ml of water and the white precipitate was dissolved. The organic layer was then washed with water (2×150 ml), 150 ml of brine and dried over MgSO4. The solvent was evaporated under vacuum to give the crude product which was recrystallized from ethyl acetate to afford 41.5 g (82%) yellow crystalline 2-nitro-4-chloro-6-bromophenol. 1H NMR (300 MHz, CDCl3) δ8.11 (d, J=2.5 Hz, 1 H), 7.87 (d, J=2.5 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613786B2
Source datasetuspto-grants-2003_09
ORD IDord-7e7a878792454987bae4ff2badb92b45
Source noteuspto-grants-2003_09