HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dibenzylamine → Urea, N'-(3-bromophenyl)-N,N-bis(phenylmethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dibenzylamine | HCID 7656 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | phenyl N-(3-bromophenyl)carbamate | HCID 885442 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Urea, N'-(3-bromophenyl)-N,N-bis(phenylmethyl)- | HCID 3867137 | — |
Reaction Steps
A solution of 1.46 g. of phenyl N-(3-bromophenyl)carbamate in 15 ml. of tetrahydrofuran is added to a solution of 2.32 g. of dibenzylamine in 20 ml. of tetrahydrofuran and the mixture is stirred under reflux for 24 hours. The mixture is diluted with hexane and the precipitate collected by filtration. Recrystallization from pentane affords 1,1-di-benzyl-3-(3-bromophenyl)urea, m.p. 102°-103° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04387106 |
| Source dataset | uspto-grants-1983_06 |
| ORD ID | ord-f1343035a7e64c9cb4f6554d3e6e8c57 |
| Source note | uspto-grants-1983_06 |