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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65821Generated: October 24, 2026

Pyridine → N'-[4-(4-tert-butylphenethyloxy)phenyl]-N-methoxy-N-methylurea

https://huagongshe.com/en/reaction/65821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEinecs 211-027-4HCID 69401—
ReactantN-methoxy-N-methylcarbamoyl chlorideHCID 2734926—
Reactant4-(4-Tert-butylphenethyloxy)anilineHCID 22756001—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductN'-[4-(4-tert-butylphenethyloxy)phenyl]-N-methoxy-N-methylureaHCID 2275600526.1%

Reaction Steps

A mixture of 26.9 g of 4-(4-tert-butylphenethyloxy)aniline, 13 g of N-methoxy-N-methylcarbamyl chloride, 10 ml of pyridine and 300 ml of toluene is heated under reflux for 7 hours. Thereafter, water is added to dissolve pyridinium chloride, and the separated toluene layer is washed with dilute hydrochloric acid, thoroughly washed with water and dried over anhydrous sodium sulfate. The solvent is then removed under reduced pressure, and the crude crystals obtained are repeatedly recrystallized from ethanol to obtain 9.3 g of N'-[4-(4-tert-butylphenethyloxy)phenyl]-N-methoxy-N-methylurea as white needles, M.P. 14°-15° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04129436
Source datasetuspto-grants-1978_12
ORD IDord-af08b02af2aa4bca8204bcf5fa2b9ff0
Source noteuspto-grants-1978_12