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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362818Generated: October 30, 2026

Malononitrile → [4-(2-Azidoethoxy)benzylidene]malononitrile

https://huagongshe.com/reaction/2362818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalononitrileHCID 8010—
ReactantPiperidineHCID 8082—
Reactant4-(2-Azidoethoxy)benzaldehydeHCID 17922552—
SolventEthanolHCID 702—
Product[4-(2-Azidoethoxy)benzylidene]malononitrileHCID 86624335—

Reaction Steps

47 μl (0.47 mmol) of piperidine are added dropwise to a solution of 3.02 g (15.79 mmol) of the compound from Example 36A and 1.09 g (16.42 mmol) of malonodinitrile in 100 ml of ethanol, and the reaction mixture is stirred at +78° C. for 3.5 h. During this time, the colour of the solution changes to orange-red. After cooling to RT, the solution is allowed to stand without stirring for 20 h. A colourless precipitate is formed. Using a rotary evaporator, the crude suspension is concentrated to half of its original volume, and the crystallization is completed with cooling in an ice bath. The resulting precipitate is filtered off with suction and washed twice with in each case 20 ml of ethanol and twice with in each case 20 ml of methyl tert-butyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691850B2
Source datasetuspto-grants-2014_04
ORD IDord-b94ffd6381404fde9236d265cd0fd221
Source noteuspto-grants-2014_04