HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848556Generated: October 30, 2026
Maleic Anhydride → HCID 86738052, compound
https://huagongshe.com/reaction/848556
Participants
| Role | Name | HCID | Charge |
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| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | HCID 54502184 | HCID 54502184 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86738052 | HCID 86738052 | — |
Reaction Steps
A stirred solution of 1.0 g. of the N-(1-methyldecyl)-3-(3-aminophenyl)-2-butenamide from Preparation 28 in 25 ml. of toluene was heated on a steam bath, and then 0.32 g. of maleic anhydride was added in one portion. After 3 minutes, the reaction mixture was cooled and the solvent was removed by evaporation in vacuo. The residue was triturated under a mixture of petroleum ether and acetonitrile, and the resulting solid was recrystallized from acetonitrile. This afforded 0.68 g. of the title compound as a light yellow solid, m.p. 126°-128° C. The IR spectrum (KBr disc) showed absorptions at 3333, 2941, 1724, 1639, 1587 and 1563 cm-1. The NMR spectrum (DMSO-d6) showed absorptions at 0.81 (s, 3H), 0.91 (s, 3H), 1.17 (s, 16H), 2.02 (m, 3H), 3.58 (m, 1H), 5.90 (d, 1H), 6.38 (m, 2H), 7.26 (m, 6H) and 10.40 (s, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04296129 |
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| Source dataset | uspto-grants-1981_10 |
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| ORD ID | ord-3cb972ddb6754072ae5841a98762cb37 |
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| Source note | uspto-grants-1981_10 |
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