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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650485Generated: 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/650485

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 P13) are introduced into 80 ml of tetrachloroethane. A total of 25.2 g of phosphorus oxybromide (POBr3) is added in portions to the brown suspension. The mixture is then stirred for 2 hours at an internal temperature of 130° C., after which it is cooled and, with cooling with an ice-bath, 150 ml of a 2M sodium hydroxide solution are added dropwise. After the addition of diethyl ether and separation of the phases, the organic phase is washed in succession with water, dilute hydrochloric acid and brine, dried over sodium sulfate, filtered and concentrated to dryness in vacuo. 19.94 g of a brown solid (crude product) are obtained, which is purified by means of digestion with 50 ml of n-hexane. 12.65 g of the desired compound are obtained in the form of a brown solid having a melting point of 110-111° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274536B1
Source datasetuspto-grants-2001_08
ORD IDord-aeff02ef1fb2438ea6c661311cbfd03c
Source noteuspto-grants-2001_08