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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732997Generated: October 30, 2026

Sulfuryl chloride → 2-[3-Chloro-4-(4-chloropyrazol-1-yl)phenyl]propionic acid

https://huagongshe.com/reaction/1732997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
Reactant2-[3-Chloro-4-(pyrazol-1-yl)phenyl]propionic acidHCID 20303500—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product2-[3-Chloro-4-(4-chloropyrazol-1-yl)phenyl]propionic acidHCID 2030341091.2%

Reaction Steps

2.5 g (10 mmoles) of 2-[3-chloro-4-(pyrazol-1-yl)phenyl]propionic acid are dissolved in 30 ml of methylene chloride. A solution of 2.01 g (15 mmoles) of sulfuryl chloride in 10 ml of chloroform is added dropwise, with cooling to the resulting solution; heating is effected gradually to room temperature; and this is followed by boiling under reflux for 2 hours. The reaction solution is allowed to cool; the solvent is distilled off; 50 ml of 2 N solution of sodium hydroxide are added to the thus-obtained residue, and boiling up is effected for a few minutes. The reaction solution is extracted with diethyl ether and then acidified with hydrochloric acid. After renewed extraction with diethyl ether, the combined ether phases are dried and evaporated to produce 2.6 g (90% of theory) of 2-[3-chloro-4-(4-chloropyrazol-1-yl)phenyl]propionic acid, m.p. 102° to 103° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04239901
Source datasetuspto-grants-1980_12
ORD IDord-c44ff154f4b14c3db056570dcd02fc88
Source noteuspto-grants-1980_12