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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265624Generated: October 25, 2026

Pyridine → 1-[2-Chloro-4-(3-chlorophenoxy)phenoxy]-2-[N-ethyl-N-(4-chlorophenylsulfenyl)aminocarbonyloxy]ethane

https://huagongshe.com/reaction/265624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTolueneHCID 1140—
Reactant4-ChlorobenzenesulfenylchlorideHCID 11084465—
ReactantHCID 20088570HCID 20088570—
SolventDiethyl EtherHCID 3283—
Product1-[2-Chloro-4-(3-chlorophenoxy)phenoxy]-2-[N-ethyl-N-(4-chlorophenylsulfenyl)aminocarbonyloxy]ethaneHCID 19034577—

Reaction Steps

A solution of 2 g of 4-chlorophenylsulfenyl chloride in 1 0 ml of toluene is added dropwise with stirring at 0°-5° C. in the course of approximately 30 minutes to a mixture of 3.7 g of 1-[2-chloro-4-(3-chlorophenoxy)phenoxy]2-ethylaminocarbonyloxyethane, 10 ml of pyridine and 10 ml of toluene, and stirring is continued for 16 hours at room temperature. The reaction mixture is diluted with 100 ml of ether, washed three times using ice-cold 1N hydrochloric acid and three times using water, the organic phase is dried over sodium sulfate and the solvent is evaporated in vacuo. The crude product is purified on silica gel using diethyl ether/n-hexane (1:3) as mobile phase. This gives the title compound of refractive index nD20 1.6209.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05648494
Source datasetuspto-grants-1997_07
ORD IDord-f3ec063891e54068a8275cf34cb46b2c
Source noteuspto-grants-1997_07