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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzenesulfenyl chloride | HCID 11008040 | — |
| Reactant | Ethyl 2-[4-(3,5-difluorophenoxy)phenoxy]ethylcarbamate | HCID 13502190 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | ethyl N-phenylthio-2-[4-(3,5-difluorophenoxy)phenoxy]ethylcarbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05192803 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-1aa673f0546042899966545ca3e52327 |
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| Source note | uspto-grants-1993_03 |
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