HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → Triphenylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N,N-Diphenylcarbamic chloride | HCID 65741 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Triphenylurea | HCID 597994 | — |
Reaction Steps
Diphenylcarbamic chloride (23 g, 0.1 mol, Aldrich Chemical Co., Milwaukee, Wis., U.S.A.) was added to a solution of 10.1 g of triethylamine and 9.3 g (0.1 mol) of benzeneamine in 150 ml of chloroform. The resulting solution was heated under reflux overnight. The solution was cooled to room temperature and washed three times with 100-ml portions of brine solution, dried over anhydrous magnesium sulfate, and evaporated to give an off-white solid which was triturated with diethyl ether to give triphenylurea as a white solid, mp 136°-138° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04797419 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-d0da4c46074645c0b6ec3f4518e0b394 |
| Source note | uspto-grants-1989_01 |