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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532575Generated: October 29, 2026

1,1,1,2-Tetrachloroethane → 3-(3-Fluoro-5-chloro-2-pyridyl)-5-bromo-1-methyl-[1H]-pyrazole

https://huagongshe.com/reaction/1532575

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1,2-TetrachloroethaneHCID 12418—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxybromideHCID 24613—
ReactantHCID 178481771HCID 178481771—
SolventDiethyl EtherHCID 3283—
Product3-(3-Fluoro-5-chloro-2-pyridyl)-5-bromo-1-methyl-[1H]-pyrazoleHCID 2171212278.1%

Reaction Conditions

Temperature130 °C

Reaction Steps

20.0 g of 3-(3-fluoro-5-chloro-2-pyridyl)-5-hydroxy-1-methyl-[1H]-pyrazole (Example H14) are initially introduced into 80 ml of tetrachloroethane. A total of 25.2 g of phosphorus oxybromide (POBr3) are added in portions to the brown suspension and the mixture is then stirred at a temperature of 130° C. for 2 hours. Thereafter, it is cooled and 150 ml of a 2 molar sodium hydroxide solution are added dropwise, while cooling with an ice-bath. After addition of diethyl ether and separation of the phases, the organic phase is washed successively with water, dilute hydrochloric acid and brine, dried over sodium sulfate, filtered and concentrated in vacuo. 19.94 g of a brown solid are obtained as the crude product, and this solid is purified by means of digestion with 50 ml of n-hexane. 12.65 g of the desired title compound are obtained as a brown solid of melting point 110-111° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204221B1
Source datasetuspto-grants-2001_03
ORD IDord-1f18caf9a05d4a5f9564df1615132eaa
Source noteuspto-grants-2001_03