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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577946Generated: November 2, 2026

Methyl iodide → 3-[3-Chloro-4-(phenethyloxy)phenyl]-1,1,3-trimethylurea

https://huagongshe.com/reaction/1577946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant3-[3-Chloro-4-(phenethyloxy)phenyl]-1,1-dimethylureaHCID 12942080—
ReactantHCID 178418361HCID 178418361—
SolventTetrahydrofuranHCID 8028—
Product3-[3-Chloro-4-(phenethyloxy)phenyl]-1,1,3-trimethylureaHCID 20566560—

Reaction Steps

A mixture of sodium hydride (0.48 g; 0.01 mol as 50% dispersion in oil) and THF (25 ml) is prepared and maintained under a nitrogen atmosphere. Then 3-[3-chloro-4-(phenethyloxy)phenyl]-1,1-dimethylurea (3.19 g; 0.01 mol) is added to the above mixture. Hydrogen is evolved and a thick paste forms. After about 15 minutes methyl iodide (1.4 g; 0.01 mol) is added and the reaction mixture stirred for two hours at room temperature. After two hours reaction time the paste redissolves. Next, most of the THF is removed under vacuum, the residue dissolved in methylene chloride. The methylene chloride solution is washed with water, dried over sodium sulfate and evaporated to afford the title product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04289903
Source datasetuspto-grants-1981_09
ORD IDord-85a6c12f53584df7ad90440c0bf97ed4
Source noteuspto-grants-1981_09