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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351950Generated: October 31, 2026

2-Nitrobenzaldehyde → HCID 14676007, compound

https://huagongshe.com/reaction/2351950

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitrobenzaldehydeHCID 11101—
ReactantHexyl acetoacetateHCID 83577—
ReactantHCID 55280984HCID 55280984—
SolventEthanolHCID 702—
ProductHCID 14676007HCID 1467600729.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04874773
Source datasetuspto-grants-1989_10
ORD IDord-4eb28a0b4db041c19ac219c75ab11861
Source noteuspto-grants-1989_10