HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 3-(3-Nitro-4-aminobenzoyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 3-(3-Nitro-4-chlorobenzoyl)pyridine | HCID 21432600 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(3-Nitro-4-aminobenzoyl)pyridine | HCID 21432587 | — |
Reaction Steps
A suspension of 63 g. (0.24 mol) of 3-(3-nitro-4-chlorobenzoyl)pyridine in 3 liters of a saturated solution of ammonia in ethanol was autoclaved at 100° C. for 24 hours. The mixture was concentrated in vacuo and the resulting residue dissolved in 1.5 liters of warm 5N HCl. The solution was cooled to room temperature and neutralized with concentrated ammonium hydroxide. The resulting product was collected as yellow-orange prisms, mp. 229° -230° C. (dimethylformamide-2-propanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04026936 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-cec53df07eca460888cad9af9ad2a29e |
| Source note | uspto-grants-1977_05 |