HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 4-Amino-3-methyl-5-nitrobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | n-(4-Cyano-2-methyl-6-nitro-phenyl)-2,2,2 trifluoro-acetamide | HCID 22021502 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Amino-3-methyl-5-nitrobenzonitrile | HCID 22021007 | 99.9% |
Reaction Steps
A mixture of N-(4-cyano-2-methyl-6-nitro-phenyl)-2,2,2-trifluoro-acetamide (5 g, 18.3 mmol) and 2 M ammonia in methanol (80 mL) was heated to reflux for 14 h and then cooled to room temperature. After concentration in vacuo, the residue was purified by flash chromatography (20% EtOAc/hexane) to yield the title compound (3.24 g, 100%, ca 80% pure). 1H NMR (300 MHz, CDCl3) δ 8.40 (1H, s), 7.47 (1H, s), 6.6-6.8 (2H, broad s), 2.89 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07312215B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-3c9b698961a242d984b704fb83c86618 |
| Source note | uspto-grants-2007_12 |