HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 2-Amino-3,5-dinitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2-Chloro-3,5-dinitropyridine | HCID 75738 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Amino-3,5-dinitropyridine | HCID 504340 | 97% |
Reaction Steps
2-Chloro3,5-dinitropyridine (2 g, 9.83 mmol) was suspended in EtOH (15 mL) and NH4OH (28% aq., 6 mL) was added dropwise over 20 minutes with stirring at room temperature. The mixture was stirred for an additional 20 minutes at room temperature and then cooled to 0° C. in an ice bath. The resulting yellow solid was collected by filtration and dried in vacuo at 80° C. to yield 1.745 g (9.5 mmol, 97%) of yellow solid. 1H NMR (500 MHz, DMSO-d6) δ 8.69 (br s, 1H), 8.96 (d, J=2.83 Hz, 1H), 9.17 (d, J=2.06 Hz, 1H), 9.26 (br s, 1H). EIMS M+1 185.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07256287B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-6bc6941540f742a38410bd7187002aba |
| Source note | uspto-grants-2007_08 |