HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351950Generated: October 31, 2026
2-Nitrobenzaldehyde → HCID 14676007, compound
https://huagongshe.com/reaction/2351950
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Reactant | Hexyl acetoacetate | HCID 83577 | — |
| Reactant | HCID 55280984 | HCID 55280984 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14676007 | HCID 14676007 | 29.9% |
Reaction Steps
o-Nitrobenzaldehyde (3.8 g, 0.025 mole), n-hexyl acetoacetate (4.6 g, 0.025 mole) and 3-aminocrotonic isopropylamide (3.5 g, 0.025 mole) are dissolved in ethanol (50 ml), and the mixture is refluxed for 8 hours. After the reaction, the solvent is distilled off under reduced pressure. The residue is dissolved in elution solvent [chloroform:carbon tetrachloride:ethyl formate:formic acid:ethanol (10:10:8:1:2)] (30 ml) and subjected to column chromatography [silica gel 60 Art. 9385 (Manufactured by Merck Co.), 300 g, φ40 mm×50 cm]. The fraction containing the desired compound is regulated to pH 10 with 28% aqueous ammonia, and the organic layer is separated, washed with water, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue is recrystallized from 80% ethanol to give the title compound (3.31 g, yield 29.9%) as yellow prisms, m.p. 175°-178° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04874773 |
|---|
| Source dataset | uspto-grants-1989_10 |
|---|
| ORD ID | ord-4eb28a0b4db041c19ac219c75ab11861 |
|---|
| Source note | uspto-grants-1989_10 |
|---|