HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Aminovaleric acid → HCID 2049944, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Aminovaleric acid | HCID 138 | — |
| Reactant | 3-Nitrophthalic anhydride | HCID 21631 | — |
| Product | HCID 2049944 | HCID 2049944 | 73% |
Reaction Steps
3-nitrophthalic anhydride (0.5 g, 0.0026 mol) and 5-aminopentanoic acid (0.30 g, 0.0026 mol) were refluxed as above overnight. The clear solution was purified as per 120 to yield 0.55 g (73%) 123 as pale yellow flat crystals: mp=158-160° C.; Rf0.69 (A): Rf0.90 (C): Rf0.73 (D): 1H NMR (DMSO-d6) δ1.53 (m, 2H), 1.58 (m, 2H), 2.24 (t, J=7.1 Hz, 2H), 3.57 (t, J=6.7 Hz, 2H), 8.04 (dd, J=8.0, 7.5 Hz, 1H), 8.16 (d, J=7.5 Hz, 1H), 8.27 (d, J=8.0 Hz, 1H); IR (cm−1): 2800-3130 (OH), 3096 (C═CH), 2691 (C—H), 1774 (C═O), 1723 (bs, C═O), 1616 (C═C), 1543 (N═O), 1466 (C═C), 1443 (C═C), 1396 (C—O), 1358 (N═O), 1209 (C—O), 1050 (C—O), 722 (C═CH); MS m/z (rel intensity) 291 (92), 247 (31), 191 (100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06468990B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-6b72077b36cb461fb78d48bb05db39ec |
| Source note | uspto-grants-2002_10 |