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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253716Generated: November 1, 2026

Butanal → Hexanoic acid, 2-cyano-, ethyl ester

https://huagongshe.com/reaction/2253716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanalHCID 261—
ReactantEthyl cyanoacetateHCID 7764—
ReactantPiperidineHCID 8082—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHexanoic acid, 2-cyano-, ethyl esterHCID 98011—

Reaction Steps

323 g of butyraldehyde and 422 g of ethyl cyanoacetate are dissolved in 750 ml of glacial acetic acid, 15 g of piperidine are added, and the reaction mixture is stirred, during which it warms to about 55° C. After the reaction mixture has been cooled to room temperature, 20 g of 5% Pd-C catalyst are added, and the mixture is then hydrogenated at 30° and an H2 pressure of 2 bar until the calculated amount of hydrogen has been taken up (about 7 hours). After the catalyst has been separated off, the hydrogenation solution is evaporated on a rotary evaporator, the residue is taken up in..methyl tertiary-butyl ether (MTB ether), and the solution is washed by shaking twice with water and subsequently with 5% NaHCO3 solution. The organic phase is dried and evaporated. The residue is distilled in vacuo (2×10-2 mbar) (62° C. to 78°), to give ethyl 2-butylcyanoacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05232624
Source datasetuspto-grants-1993_08
ORD IDord-d7f9d70ede2349108bf23d4689c3290a
Source noteuspto-grants-1993_08