Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Dichloronitrobenzene | HCID 11899 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10634737 | HCID 10634737 | 19.1% |
Reaction Steps
A mixture of 15.09 g (78 mmol) 2,4-dichloronitrobenzen, 7.7 g (78 mmol) cyclohexylamine, 7.9 g (78 mmol) triethylamine and 100 ml dimethylformamide was stirred at 80° C. for 3 h. After cooling to 25° C. the mixture was evaporated, dissolved in 200 ml ether and filtered. The ether solution was washed with water and evaporated to the half volume. The precipitate was filtered off to give 3.8 g (19%) N-cyclohexyl-2-nitro-5-chloraniline. M.p. 124.5° C. 1H-NMR (CDCl3): 8.2 (2H, m), 6.8 (1H, d), 6.5 (1H, dd), 3.5 (1H, broad s), 2.4-0.8 (10H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05026704 |
|---|
| Source dataset | uspto-grants-1991_06 |
|---|
| ORD ID | ord-46c76f41ab0e48f3994f2be16a80487d |
|---|
| Source note | uspto-grants-1991_06 |
|---|