Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408538Generated: October 27, 2026

Acetic Acid → (2E)-2-(1H-Indazol-5-ylmethylidene)-3-oxobutanenitrile

https://huagongshe.com/reaction/408538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
Reactant1H-Indazole-5-carboxaldehydeHCID 21250644—
Reactantsodium (1Z)-1-cyanoprop-1-en-2-olateHCID 23687916—
CatalystPiperidineHCID 8082—
SolventDichloromethaneHCID 6344—
Product(2E)-2-(1H-Indazol-5-ylmethylidene)-3-oxobutanenitrileHCID 66725268131.5%

Reaction Steps

10 g (68.4 mmol) 1H-indazole-5-carbaldehyde [preparation described in US 2005/0227968-A1 (Intermediate 1)], 7.91 g (75.2 mmol) sodium (1Z)-1-cyanoprop-1-en-2-olate, 4.89 ml (85.5 mmol) acetic acid and 0.68 ml (6.84 mmol) piperidine in dry dichloromethane (500 ml) were stirred at reflux temperature for 7 h using an inverse water separator. Upon cooling, a precipitate was formed which was collected by filtration and washed with dichloromethane. The solid was dried in vacuo to afford the crude title compound (19 g, 75% purity by LC-MS, 96% of th.) which was used in subsequent steps without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759341B2
Source datasetuspto-grants-2014_06
ORD IDord-9dfe2e550edd4ae0b56c418732c2f1eb
Source noteuspto-grants-2014_06