HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → N-Butyl-N-(heptan-2-YL)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(2-Heptyl)aniline | HCID 11344519 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Butyl-N-(heptan-2-YL)aniline | HCID 18000381 | 44% |
Reaction Steps
A mixture of N-(1-methylhexyl)aniline (76 parts), 1-bromobutane (66 parts), anhydrous potassium carbonate (65 parts) and DMF (150 parts) was stirred while heating under reflux for 41 hours. An additional quantity of 1-bromo butane (44 parts) was added and the mixture stirred while heating under reflux for a further 19 hours. The cooled mixture was poured into water (400 parts) and the organic phase separated. The aqueous phase was extracted with toluene, the organic phases and toluene extract were combined and washed with water (2×100 parts) before evaporating to leave N-butyl-N-(1-methylhexyl)aniline (72.8 parts, 44%) which was purified by vacuum distillation to give N-butyl-N-(1-methylhexyl)aniline b.pt 73-80° C., 2.6 mm Hg. [Dye (1)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06641620B1 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-65cd0450302f40a4a7683d7e9e12f3f4 |
| Source note | uspto-grants-2003_11 |