HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-4-nitroaniline → 2-Methyl-N-(2-methyl-4-nitrophenyl)acrylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-4-nitroaniline | HCID 7441 | — |
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Product | 2-Methyl-N-(2-methyl-4-nitrophenyl)acrylamide | HCID 45097641 | — |
Reaction Steps
2-Methyl-N-(2-methyl-4-nitrophenyl)acrylamide was prepared as described in Example 1a starting from 2-methyl-4-nitroaniline and methacryloyl chloride. 1H NMR (400 MHz, DMSO-d6): 1.98 (3H, s), 2.34 (3H, s), 5.59 (1H, s), 5.91 (1H, s), 7.74 (1H, d, J=8.8 Hz), 8.07 (1H, dd, J=8.8 Hz, J=2.7 Hz), 8.15 (1H, d, J=2.6 Hz), 9.53 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07390923B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-6429a302fea4436291a646d47d1a4a68 |
| Source note | uspto-grants-2008_06 |