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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261483Generated: October 26, 2026

Methyl iodide → N-(2,6-dichlorobenzoyl)-N-(methoxymethyl)-N'-(4-chlorophenyl)-urea

https://huagongshe.com/reaction/261483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantPotassium HydroxideHCID 14797—
Reactant2,6-dichloro-N-(((4-chlorophenyl)amino)carbonyl)benzamideHCID 92300—
SolventDimethylformamideHCID 6228—
ProductN-(2,6-dichlorobenzoyl)-N-(methoxymethyl)-N'-(4-chlorophenyl)-ureaHCID 19006383—

Reaction Steps

10.3 g of N-(2,6-dichlorobenzoyl)-N'-(4-chlorophenyl)-urea and 1.88 g of powdered potassium hydroxide (90%) are dissolved 40 ml of dimethyl formamide, after which 4.7 g of methyl iodide are added drop by drop to the clear solution. The resulting reaction is exothermic. After stirring for two hours the solution is diluted with ice water and the solid substance is isolated. Yield 10.3 g. Melting point 124°-126° C. In a completely similar manner but using methoxymethylchloride instead of methyliodide, N-(2,6-dichlorobenzoyl)-N-(methoxymethyl)-N'-(4-chlorophenyl)-urea is produced. Melting point 121.5°-122.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04166124
Source datasetuspto-grants-1979_08
ORD IDord-07b19747ba954b9a81e9a1d40b73b9f9
Source noteuspto-grants-1979_08