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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322188Generated: October 27, 2026

Acetic Acid → 7-Azido-2-[(4-nitrophenyl)methylene]-3-oxoheptanoic acid 2-cyanoethyl ester

https://huagongshe.com/reaction/322188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCarbon DioxideHCID 280—
Reactant4-NitrobenzaldehydeHCID 541—
ReactantHydracrylonitrileHCID 8011—
ReactantPiperidineHCID 8082—
Reactant5-(5-Azidopentanoyl)-2,2-dimethyl-1,3-dioxane-4,6-dioneHCID 23004073—
SolventIsopropanolHCID 3776—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product7-Azido-2-[(4-nitrophenyl)methylene]-3-oxoheptanoic acid 2-cyanoethyl esterHCID 53869981—

Reaction Steps

5-(5-Azidopentanoyl)-2,2-dimethyl-1,3-dioxane-4,6-dione was heated with 3-hydroxypropionitrile (2.42 g, 34.0 mmol) at 80° C. until no more CO2 was released. After cooling to room temperature, the mixture was diluted with 150 ml of 2-propanol, and 4-nitrobenzaldehyde (4.60 g, 30.3 mmol), piperidine (130 mg, 1.50 mmol) and acetic acid (90 mg, 1.50 mmol) were added. The mixture was stirred at room temperature for 48 hrs. The product, 7-azido-2-[(4-nitrophenyl)methylene]-3-oxoheptanoicacid2-cyanoethyl ester was obtained as a pale-yellow oil (5.73 g, 51% yield) after chromatography (SiO2, Hexane: AcOEt, 2:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211198B1
Source datasetuspto-grants-2001_04
ORD IDord-a7ed828c3a644913b50194ade03649ce
Source noteuspto-grants-2001_04