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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490561Generated: November 1, 2026

Acrylonitrile → HCID 68838102, compound

https://huagongshe.com/reaction/490561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-Dihydro-5-nitro-1H-indazol-3-oneHCID 5374661—
SolventWaterHCID 962—
ProductHCID 68838102HCID 68838102—

Reaction Conditions

Temperature50 °C

Reaction Steps

5-Nitro-1,2-dihydro-indazol-3-one (prepared according to Org. Synth. 1949, 29, 54 or Chem Ber. 1942, 75, 1104) (0.6 g) was suspended in water (8 mL) and 2N K2CO3 (aq.) (1.8 g) was added to the flask and the mixture was heated to 50° C. for 10 minutes. Acrylonitrile (0.24 mL) was then added dropwise. The reaction was stirred overnight and was quenched with 2 N HCl (aq.) solution while cooling in an ice bath. The aqueous phase was extracted with EtOAc and the combined phases were washed with brine, dried over sodium sulfate, filtered and reduced in vacuo. Flash column chromatography over silica gel (eluting with EtOAc, nheptane, 3% AcOH) afforded pure desired 3-(5-Nitro-3-oxo-2,3-dihydro-indazol-1-yl)-propionitrile as a white solid. MS (ESI+: 233.3[M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528158B2
Source datasetuspto-grants-2009_05
ORD IDord-6bfc72e327694d3bb79465eb32f927e9
Source noteuspto-grants-2009_05