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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415092Generated: November 1, 2026

Water → HCID 21391467, compound

https://huagongshe.com/reaction/1415092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactant4-ChlorobenzenesulfenylchlorideHCID 11084465—
ReactantHCID 86732873HCID 86732873—
SolventHexaneHCID 8058—
ProductHCID 21391467HCID 21391467—

Reaction Conditions

Temperature30 °C

Reaction Steps

4-Chlorobenzenesulfenyl chloride (8.68 grams; 0.0496 mole) was added over a period of about 3 minutes to a solution of N'-(4-((6-chloro-2-pyridinyl)oxy)phenyl-N-methylurea (8.3 grams; 0.03 mole) in 50 ml. of dry pyridine. The resulting reaction mixture was stirred at a temperature of about 30° C. for a period of about 1 and one-half hours and then poured into 250 ml. of cold water. The resulting sticky product precipitate was dissolved in hot hexane, reprecipitated therefrom upon standing and the light-yellow, slightly sticky product obtained triturated with a small amount of cold acetonitrile. Filtration of the mixture gave the desired N-((4-chlorophenyl)thio)-N'-(4-((6-chloro-2-pyridinyl)oxy)phenyl)-N-methylurea compound as a white crystalline solid melting at 106°-109° C. The product was found to have carbon, hydrogen, nitrogen, chlorine and sulfur contents of 54.2, 3.5, 9.86, 17.0 and 7.46 percent, respectively, as compared with contents of 54.3, 3.6, 10.0, 16.87 and 7.6 percent, respectively, as calculated for the named structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04003734
Source datasetuspto-grants-1977_01
ORD IDord-fc932979d4e64ad5baf37464c8cd0f27
Source noteuspto-grants-1977_01