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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | (2,2-Dimethoxyethyl)-(4-phenoxyphenyl)amine | HCID 21873313 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(2,2-Dimethoxyethyl)-3-(4-methoxyphenyl)-1-(4-phenoxyphenyl)urea | HCID 21873430 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07141561B2 |
|---|
| Source dataset | uspto-grants-2006_11 |
|---|
| ORD ID | ord-b6949a51fead49749a75d4ec9d09091f |
|---|
| Source note | uspto-grants-2006_11 |
|---|