HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → N'-(3-Bromophenyl)-N,N-dibutylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dibutylamine | HCID 8148 | — |
| Reactant | HCID 21920096 | HCID 21920096 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | N'-(3-Bromophenyl)-N,N-dibutylurea | HCID 20499411 | — |
Reaction Steps
A solution of 1.46 g. of phenyl N-(3-bromophenylcarbamate in 15 ml. of tetrahydrofuran is added to a solution of 1.52 g. of di-n-butylamine 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-(n-butyl)-3-(3-bromophenyl)urea, m.p. 80°-81° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04387105 |
| Source dataset | uspto-grants-1983_06 |
| ORD ID | ord-f73b2f0f28c641d4ba2658f41d63b3d7 |
| Source note | uspto-grants-1983_06 |