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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364951Generated: October 25, 2026

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

https://huagongshe.com/reaction/364951

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 numberUS04607044
Source datasetuspto-grants-1986_08
ORD IDord-0058f42e565d417d9a623d83ddd03b57
Source noteuspto-grants-1986_08