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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407652Generated: October 29, 2026

Butanal → 2-Ethylhex-2-Enal

https://huagongshe.com/reaction/2407652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanalHCID 261—
Solvent1-ButanolHCID 263—
Product2-Ethylhex-2-EnalHCID 12582—

Reaction Steps

The experiment in this example was carried out as described in Example 7 except that the first catalyst charged to the reactor was 5.02 g (6.8 mL) charge of Catalyst D; the reaction time was two hours. These results correspond to 94% butanol conversion and 57.3% conversion of theoretical butyraldehyde. Selectivities based on molar conversion of butyraldehyde: 5.6% selectivity to butylbutyrate, 54.8% selectivity to oxygenated 2-EH products and 7.0% selectivity to dehydrated 2-EH products. This example demonstrates that the Catalyst A forms only a slight amount of ester while generating butyraldehyde which undergoes aldol self-condensation over Catalyst D to form primarily 2-ethyl-2-hex-enal along with other 2-EH related compounds.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809594B2
Source datasetuspto-grants-2014_08
ORD IDord-c058ca8cb7744b4285a85e2a95a7e6f0
Source noteuspto-grants-2014_08