HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromopropane → N-(2-ethylhexyl)-N-propylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(2-Ethylhexyl)aniline | HCID 61484 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-ethylhexyl)-N-propylaniline | HCID 53707404 | 78% |
Reaction Conditions
| Temperature | 125 °C |
|---|
Reaction Steps
A mixture of N-(2-ethylhexyl)aniline (8.9 parts), 1-bromopropane (7.4 parts), anhydrous potassium carbonate (11 parts) and N,N-dimethylformamide (30 parts) was stirred at 125° C. for 24 hours. An additional quantity of 1-bromopropane (5 parts) was added and the mixture stirred for a further 18 hours at 125° C. The cooled mixture was filtered and poured into water. The product was extracted into dichloromethane and evaporated to yield N-(2-ethylhexyl)-N-propylaniline (8.9 parts, 78%) which was reacted with acetic anhydride prior to use to remove any unreacted starting materials.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05660598 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-d6483d1599d8480c890a96e246e7225f |
| Source note | uspto-grants-1997_08 |