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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376215Generated: November 1, 2026

Ethyl cyanoacetate → 5'-(2-Cyano-2-ethoxycarbonylvinyl)-1,3,3-trimethylspiro-[indoline-2,3'-[3H]-naphtho[2,1-b][1,4]oxazine]

https://huagongshe.com/reaction/376215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
Reactant5'-Formyl-1,3,3-trimethylspiro[indoline-2,3'-[3H]-naphtho[2,1-b][1,4]oxazine]HCID 15305689—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
Product5'-(2-Cyano-2-ethoxycarbonylvinyl)-1,3,3-trimethylspiro-[indoline-2,3'-[3H]-naphtho[2,1-b][1,4]oxazine]HCID 53658548—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 0.18 g (1.5 mmol) of ethyl cyanoacetate in a minimum quantity of ethanol are added 0.36 g (1 mmol) of the product of Example 1 and then two drops of piperidine. The mixture is heated at 60° C. until a precipitate appears. The precipitate obtained is filtered off, washed with ethanol and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06019914
Source datasetuspto-grants-2000_02
ORD IDord-b382f62596194f3db208fbcf87334264
Source noteuspto-grants-2000_02