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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280404Generated: October 28, 2026

Ethanol → Butanamide, N,N-diethyl-

https://huagongshe.com/reaction/280404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2-ButenaMide, N,N-diethyl-, (E)-HCID 5354453—
ReactantHCID 178418361HCID 178418361—
SolventPyridineHCID 1049—
ProductButanamide, N,N-diethyl-HCID 66192—
ProductN,N-Diethylbut-3-enamideHCID 12545744—

Reaction Steps

56.5 g of crotonic acid diethylamide 36.9 g of ethanol, 1.27 g of pyridine and 2.74 g of Co2 (CO)8 are reacted analogously to Example 1 for 1.5 hours at 170° C. under a carbon monoxide pressure of 150 bar (+approx. 2% by volume of hydrogen). Analysis showed that 99.6 mol % of the crotonic acid diethylamide had reacted. Relative to this, C5 -dicarboxylic acid derivatives containing mixed derivative groups had been formed at a selectivity of conversion of 97.4 mol %; 2-methylsuccinic acid 1-ethylester-4-diethylamide was 93.6% of this. In addition, butyric acid diethylamide and but-3-enoic acid diethylamide had been formed at selectivities of conversion of 1.2 mol % and 0.4 mol %, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04588833
Source datasetuspto-grants-1986_05
ORD IDord-d8a8898b7e9a43319fd2142c67bb9229
Source noteuspto-grants-1986_05