HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Ethyl 4-amino-5,6-heptadienoate hydrochloride salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 5,6-Heptadienoic acid, 4-amino- | HCID 10261186 | — |
| Product | Ethyl 4-amino-5,6-heptadienoate hydrochloride salt | HCID 13920715 | — |
Reaction Steps
To 4-amino-5,6-heptadienoic acid in anhydrous ethanol at 0° C. was added gaseous HCl. The reaction was left overnight at room temperature and then evacuated to a residue. This was taken in ethyl acetate, decolorized with charcoal, and then crystallization accomplished from ethyl acetate-ether to give the title compound. mp. 81°-83° C.; IR (KBr): 1952, 1710 cm-1. 'H NMR (δD2O): 1.3 (t, 3H, J=6.9 Hz, CH3), 1.9-2.8 (m, 4H, CH2CH2), 3.95 (m, 1H, CHN), 4.2 (q, 2H, J=6.9 Hz, OCH2), 5.0-5.4 (m, 3H H2C=C=CH). Anal. Calcd. for C9H16ClNO2 : C, 52.56, H, 7.84, N, 6.87; Found: C, 52.45, H, 7.95, N, 6.98.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04668703 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-41aa0a673d2b4e8c959acd2d9c05f16e |
| Source note | uspto-grants-1987_05 |