HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → N-Ethyl-3-nitro PABA
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | 4-Fluoro-3-nitrobenzoic acid | HCID 67987 | — |
| Product | N-Ethyl-3-nitro PABA | HCID 3729086 | — |
Reaction Steps
In a manner similar to Example 31, 4-fluoro-3-nitrobenzoic acid was treated with ethylamine to give 4-ethylamino-3-nitrobenzoic acid, which was then esterified with anhydrous hydrogen chloride in methanol to give the title compound. 1H-NMR (CDCl3): δ 8.89 (1H, d), 8.28 (1H, br s), 8.06 (1H, dd), 6.87 (1H, d), 3.90 (3H, s), 3.42 (2H, m), 1.40 (3H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115640B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-54fc9f9f55a644dc973e76c03ff121a9 |
| Source note | uspto-grants-2006_10 |