HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzamide → N-Butylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzamide | HCID 2331 | — |
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Butylbenzamide | HCID 76024 | — |
Reaction Steps
1-Bromobutane (1.51 g, 0.011 mol) in benzene (10 ml) was slowly added to a refluxing mixture of benzamide (1.21 g, 0.01 mol), 50% aqueous sodium hydroxide solution (10 ml) and 1 mmol of the catalyst (Table 3). After the addition of has been completed, refluxing is continued for 4 hours. The reaction mixture was then cooled to room temperature and diluted with water (20 ml). The organic phase is separated, washed with water (3×10 ml) until neutral, dried over magnesium sulphate and evaporated to give pure N-n-butylbenzamide. Yields are given in Table 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04880894 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-1517a2593f0c42d8aff2f9b3ccadd983 |
| Source note | uspto-grants-1989_11 |