HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723334Generated: October 25, 2026
4-Benzyloxyaniline → 3-(4-Benzyloxyphenyl)-1-(2,2-dimethoxyethyl)-1-(4-phenoxyphenyl)urea
https://huagongshe.com/reaction/723334
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Benzyloxyaniline | HCID 22860 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | (2,2-Dimethoxyethyl)-(4-phenoxyphenyl)amine | HCID 21873313 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(4-Benzyloxyphenyl)-1-(2,2-dimethoxyethyl)-1-(4-phenoxyphenyl)urea | HCID 21873322 | — |
Reaction Steps
A solution of 4-benzyloxyaniline (199 mg) in dimethylformamide (1 ml) was added dropwise to a solution of carbonyldiimidazole (162 mg) in dimethylformamide (1 ml) at 0° C. After a reaction time at 0° C. of 10 minutes, the reaction was allowed to continue at room temperature for 20 minutes. Then (2,2-dimethoxyethyl)-(4-phenoxyphenyl)amine (273 mg) was added, and the mixture was heated at 80° C. for 1.5 hours. Cooling was followed by dilution with water and extraction with ethyl acetate. The organic phase was dried over magnesium sulfate and concentrated. The product with the molecular weight of 498.58 (C30H30N2O5); MS (ESI): 499 ([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-0f11f72f476a4292a628fef156f83830 |
|---|
| Source note | uspto-grants-2006_11 |
|---|