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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358479Generated: October 30, 2026

Hydrochloric Acid → HCID 13373522, compound

https://huagongshe.com/reaction/358479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl formateHCID 8025—
ReactantSodium hydrideHCID 24758—
Reactant3-Pyridinebutanoic acid, ethyl esterHCID 11679975—
SolventDimethylformamideHCID 6228—
ProductHCID 13373522HCID 13373522—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 2.53 g. of sodium hydride in 35 ml. of anhydrous dimethyl formamide was prepared. The suspension was cooled to about 0° C. with stirring. Next, a mixture of 9.56 g. of ethyl formate and 19 g. of ethyl 4-(3-pyridyl)butyrate were added. The consequent reaction mixture was stirred at about 0° C. for 1 additional hour and then at room temperature for about 3 days. The reaction mixture was acidified with 2N aqueous hydrochloric acid and the acidic aqueous solution evaporated to a very small volume in vacuo. The acidity of the solution was adjusted to pH=6 by the addition of solid potassium carbonate. The neutral aqueous layer was then extracted with ether. The ether layer was separated and dried. Evaporation of the ether yielded 16.4 g. of ethyl 2-formyl-4-(3-pyridyl)butyrate (formed in the above reaction) as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04468399
Source datasetuspto-grants-1984_08
ORD IDord-5f89918373ff4aaf9f5f5c61206f441e
Source noteuspto-grants-1984_08