HuagongsheHuagongshe Chemistry Print Report · For research reference only
Maleic Anhydride → N-Decyl-3-(3-[cis-3-carboxypropenamido]phenyl)propenamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | N-decyl-3-(3-aminophenyl)propenamide | HCID 53861940 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-Decyl-3-(3-[cis-3-carboxypropenamido]phenyl)propenamide | HCID 86738051 | — |
Reaction Steps
A stirred mixture of 0.907 g. of N-decyl-3-(3-aminophenyl)propenamide and 25 ml. of benzene was heated on a steam bath until a solution was obtained. To this solution was then added 0.358 g. of maleic anhydride in one portion. In about 30 seconds a solid precipitated. The mixture was allowed to cool and then the solid was recovered by filtration. The solid was recrystallized from acetic acid, to give 1.1 g. (92% yeild) of the title compound, melting point 187°-188° C. The IR spectrum (KBr disc) showed absorptions at 3279, 2899, 1724, 1653, 1626, 1587 and 1563 cm-1. The NMR spectrum (in DMSO-d6) showed absorptions at 0.91 (m, 3H), 1.24 (s, 16H), 3.18 (m, 2H), 6.50 (m, 4H), 7.42 (m, 4H), 8.11 (m, 2H) and 10.50 (s, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04296129 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-28994c12d7794456aa94f8a536bfb0d1 |
| Source note | uspto-grants-1981_10 |