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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613445Generated: October 30, 2026

Hydrochloric Acid → ethyl N-phenylthio-2-[4-(3,5-difluorophenoxy)phenoxy]ethylcarbamate

https://huagongshe.com/reaction/1613445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzenesulfenyl chlorideHCID 11008040—
ReactantEthyl 2-[4-(3,5-difluorophenoxy)phenoxy]ethylcarbamateHCID 13502190—
SolventPyridineHCID 1049—
SolventTolueneHCID 1140—
Productethyl N-phenylthio-2-[4-(3,5-difluorophenoxy)phenoxy]ethylcarbamateHCID 19775874—

Reaction Steps

5.7 g of freshly distilled phenylsulfenyl chloride in 10 ml of toluene are added dropwise at 0° to +5° C. in the course of 30 minutes to a solution of 12 g of ethyl 2-[4-(3,5-difluorophenoxy)phenoxy]ethylcarbamate in 40 ml of pyridine, with stirring. After this, the mixture is stirred for 4 more hours at room temperature. The reaction mixture is poured into 300 ml of 2N hydrochloric acid and ice, and the mixture is extracted twice using diethyl ether. The combined organic phases are washed to neutrality with water and sodium chloride solution and dried over sodium sulfate. The solvent is distilled off in vacuo, and the residue is purified by chromatography on silica gel (eluent: hexane/diethyl ether, 20:1), which gives pure ethyl N-phenylthio-2-[4-(3,5-difluorophenoxy)phenoxy]ethylcarbamate, nD20 : 1.5700.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192803
Source datasetuspto-grants-1993_03
ORD IDord-1aa673f0546042899966545ca3e52327
Source noteuspto-grants-1993_03