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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415093Generated: November 1, 2026

Sodium Hydroxide → N'-(4-((6-chloro-2-pyridinyl)oxy)phenyl)-N,N-dimethyl urea-1-oxide

https://huagongshe.com/reaction/1415093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2,6-Dichloropyridine N-OxideHCID 817673—
ReactantUrea, N'-(4-hydroxyphenyl)-N,N-dimethyl-HCID 3014146—
SolventDimethyl SulfoxideHCID 679—
ProductN'-(4-((6-chloro-2-pyridinyl)oxy)phenyl)-N,N-dimethyl urea-1-oxideHCID 21391435—

Reaction Conditions

Temperature60 °C

Reaction Steps

Dry powdered sodium hydroxide (2.44 grams; 0.061 mole) was dissolved in 110 ml. of warm dimethylsulfoxide and N'-(4-hydroxyphenyl)-N,N-dimethyl urea (11.0 grams; 0.061 mole) and 2,6-dichloropyridine-N-oxide added thereto. The reaction mixture was stirred at a temperature of about 60° C. for a period of 5 and one-half hours. After this period, about three-fourths of the solvent carrier was removed by vacuum distillation and the residual oil thus obtained poured into ice water. The aqueous mixture was extracted with three 250 ml. portions of warm methylene chloride and the extracts combined. Evaporation of the solvent from the extract left a brown, syrupy residue which was washed with cold water and then with dry benzene to give the desired N'-(4-((6-chloro-2-pyridinyl)oxy)phenyl)-N,N-dimethyl urea-1-oxide compound as a crystalline solid melting at 190°-191° C. and having carbon, hydrogen, nitrogen and chlorine contents of 53.83, 4.63, 13.25 and 12.78 percent, respectively, as compared with contents of 54.64, 4.58, 13.65 and 11.52 percent, respectively, calculated for the named structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04003734
Source datasetuspto-grants-1977_01
ORD IDord-097c7a80e81f48928ffb23c8d638efe1
Source noteuspto-grants-1977_01