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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600864Generated: October 31, 2026

Ethyl orthoformate → Ethyl 2-(2,6-dichloropyridine-3-carbonyl)-3-ethoxyprop-2-enoate

https://huagongshe.com/reaction/600864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantEthyl 3-(2,6-dichloropyridin-3-YL)-3-oxopropanoateHCID 44140080—
SolventAcetic AnhydrideHCID 7918—
ProductEthyl 2-(2,6-dichloropyridine-3-carbonyl)-3-ethoxyprop-2-enoateHCID 54146668—

Reaction Conditions

Temperature140 °C

Reaction Steps

Ethyl 2-(2,6-dichloronicotinoyl)acetate (7.03 g, 26.8 mmol) was dissolved in acetic anhydride (30 ml), and after adding triethyl orthoformate (60 ml) thereto, it was stirred in an oil bath of 140° C. for 2 hours. After letting the reaction solution cool, it was concentrated under a reduced pressure, and after adding toluene (50 ml) to the residue obtained, a concentration operation under a reduced pressure was performed. This operation was repeated 3 times, and the residue obtained was dried under a reduced pressure. 8.42 g of ethyl 2-(2,6-dichloronicotinoyl)-3-ethoxyacrylate was thereby obtained in the form of a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902226B2
Source datasetuspto-grants-2011_03
ORD IDord-d15d8e2a789749cc9db4bfc91efb598f
Source noteuspto-grants-2011_03