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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490814Generated: October 30, 2026

Ethanol → HCID 9997363, compound

https://huagongshe.com/reaction/490814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMalononitrileHCID 8010—
ReactantIndole-3-CarboxaldehydeHCID 10256—
Reactant[(1H-Indol-3-yl)methylidene]propanedinitrileHCID 269623—
CatalystPiperidineHCID 8082—
ProductHCID 9997363HCID 999736375%

Reaction Steps

2-(Indol-3-ylmethylene)-malononitrile: A yellow suspension of malononitrile (0.114 g, 1.72 mmol), anhydrous EtOH (1.72 mL), indole-3-carboxaldehyde (0.250 g, 1.72 mmol), and piperidine (6.8 μL, 0.069 mmol) was heated to form a yellow solution. Within 5 min, a yellow precipitate was formed and the reaction mixture was cooled to room temperature over 15 min. The yellow precipitate was filtered and collected, yielding 0.250 g (75%) of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528164B2
Source datasetuspto-grants-2009_05
ORD IDord-e2553fedb72d448792b3dc49d9e92aec
Source noteuspto-grants-2009_05