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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739648Generated: November 1, 2026

Phenylphosphonic dichloride → 5-Bromo-2-chloro-3-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/1739648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylphosphonic dichlorideHCID 69990—
ReactantHCID 178517592HCID 178517592—
Product5-Bromo-2-chloro-3-(trifluoromethyl)pyridineHCID 21836302—

Reaction Conditions

Temperature135 °C

Reaction Steps

The product of Example 5 (11.5 g, 0.048 mol) and phenylphosphoryl dichloride (45 mL) were heated with stirring at 135° C. for four hours and allowed to cool to room temperature. The reaction mixture was poured onto ice (750 g) and allowed to warm to room temperature. The mixture was extracted with dichloromethane (150 mL) and filtered. The organic phase was separated, washed with water and 10% sodium carbonate solution and dried over anhydrous sodium sulphate. Evaporation of the solvent gave 2-chloro-3-trifluoromethyl-5-bromopyridine (11.6 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05968875
Source datasetuspto-grants-1999_10
ORD IDord-bc1178f62f794614881bac365465cca1
Source noteuspto-grants-1999_10