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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723339Generated: October 25, 2026

P-Anisidine → 1-(2,2-Dimethoxyethyl)-3-(4-methoxyphenyl)-1-(4-phenoxyphenyl)urea

https://huagongshe.com/reaction/723339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(2,2-Dimethoxyethyl)-(4-phenoxyphenyl)amineHCID 21873313—
SolventDimethylformamideHCID 6228—
Product1-(2,2-Dimethoxyethyl)-3-(4-methoxyphenyl)-1-(4-phenoxyphenyl)ureaHCID 21873430—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 4-methoxyaniline (1.9 g) in dimethylformamide (3 ml) was added dropwise to a solution of carbonyidiimidazole (2.51 g) in dimethylformamide (15 ml) at 0° C. After a reaction time at 0° C. of 15 minutes, the reaction was allowed to continue at room temperature for 45 minutes. Then (2,2-dimethoxyethyl)-(4-phenoxyphenyl)amine (4.1 g) in dimethylformamide (2 ml) was added, and the mixture was heated at 80° C. for 2 hours. After cooling, volatiles were removed and the residue was taken up in ethyl acetate. The organic phase was washed with water and saturated brine. The organic phase was dried over magnesium sulfate and concentrated. The product with the molecular weight of 422.49 (C24H26N2O5); MS (ESI): 423 ([M+H]+), was obtained in this way.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141561B2
Source datasetuspto-grants-2006_11
ORD IDord-b6949a51fead49749a75d4ec9d09091f
Source noteuspto-grants-2006_11