Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417647Generated: November 2, 2026

Acetic Anhydride → 4-Ethoxy-3-(4-pyridyl)-3-buten-2-one

https://huagongshe.com/reaction/2417647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl orthoformateHCID 31214—
Reactant4-PyridinylacetoneHCID 80552—
SolventAcetic AcidHCID 176—
Product4-Ethoxy-3-(4-pyridyl)-3-buten-2-oneHCID 3021227—

Reaction Steps

The process according to claim 2 where 4-pyridinylmethyl methyl ketone is first reacted with triethyl orthoformate, acetic anhydride and acetic acid to produce 2-ethoxy-1-(4-pyridinyl)ethenyl methyl ketone, said latter ketone is reacted with cyanoacetamide in the presence of at least a molar equivalent quantity of sodium hydroxide per mole of cyanoacetamide in methanol and the reaction mixture is neutralized to produce 1,2-dihydro-6-methyl-2-oxo-5-(4-pyridinyl)nicotinonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04469871
Source datasetuspto-grants-1984_09
ORD IDord-f0df5abe32624c84a5778ee775c05f02
Source noteuspto-grants-1984_09