HuagongsheHuagongshe Chemistry Print Report · For research reference only
trans-N-Octyl-2-(4-nitrophenyl)cyclopropanecarboxamide → trans-N-octyl-2-(4-aminophenyl)cyclopropanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | trans-N-Octyl-2-(4-nitrophenyl)cyclopropanecarboxamide | HCID 12854633 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | trans-N-octyl-2-(4-aminophenyl)cyclopropanecarboxamide | HCID 12854635 | — |
Reaction Steps
To a stirred solution of 6.2 g. of trans-N-octyl-2-(4-nitrophenyl)cyclopropanecarboxamide in 70 ml. of glacial acetic acid, at 85° C., was added 5.3 g. of iron powder, portionwise, during 10 minutes. The temperature was kept between 85° and 90° C. during the addition. At the end of the addition, stirring was continued at 85°-90° C. for 10 minutes, and then the hot reaction mixture was filtered. The filtrate was evaporated in vacuo, and the residue thus obtained was partitioned between 350 ml. of ethyl acetate and 150 ml. of saturated sodium chloride solution. The ethyl acetate layer was removed, dried using sodium sulfate, and evaporated in vacuo. This gave 5.4 g. of the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04331683 |
| Source dataset | uspto-grants-1982_05 |
| ORD ID | ord-2094a272cb414ea3839746e0bbc318a5 |
| Source note | uspto-grants-1982_05 |