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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045121Generated: October 25, 2026

Butanal → 2-Ethylhex-2-Enal

https://huagongshe.com/reaction/1045121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanalHCID 261—
SolventWaterHCID 962—
Product2-Ethylhex-2-EnalHCID 12582—

Reaction Steps

The aldol reaction of n-butyraldehyde with simultaneous elimination of water to form 2-ethylhexenal is carried out worldwide on a large scale since the hydrogenation product, viz. 2-ethylhexanol, is used in large quantities as plasticizer alcohol. As catalyst, use is usually made of a base dissolved in water. The use of aqueous sodium hydroxide having an NaOH content in the percentage range is typical. The reaction is frequently carried out in a temperature range of 80-150° C., a pressure of less than 5 bar and a phase ratio of organic phase to aqueous catalyst phase of from 1 to 20 (Hydrocarbon Processing, October 1980, Section 2, pages 93-102). This reaction can, for example, be carried out in a stirred vessel (DE 19 06 850, DE 927 626), in a packed column which is operated in countercurrent (G. Dümbgen, D. Neubauer, Chemie-Ing.-Techn., 41, 974 (1969)), or in a flow tube (GB 761 203). All these processes give 2-ethylhexenal in a selectivity of up to 98% at conversions of 98.5%. A disadvantage is that at relatively high temperatures, part of the n-butyraldehyde used is irreversibly lost as a result of the Cannizzaro reaction. The butyric acid formed in the Cannizzaro reaction neutralizes the basic catalyst. Part of the catalyst solution containing a high burden of organic material therefore has to be continually discharged and replaced by fresh catalyst.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563782B2
Source datasetuspto-grants-2013_10
ORD IDord-bb73726800a5448ea3131980c01b7d07
Source noteuspto-grants-2013_10