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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645463Generated: October 30, 2026

4-Acetoxybutyraldehyde → 4-Hydroxybutyl acetate

https://huagongshe.com/reaction/1645463

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AcetoxybutyraldehydeHCID 11007927—
SolventTetrahydrofuranHCID 8028—
Product4-Hydroxybutyl acetateHCID 10103209—

Reaction Steps

Alternatively, at least a portion of the 4-acetoxybutyraldehyde reaction product may be preferably converted to produce tetrahydrofuran (THF). Preferably, the 4-acetoxybutyraldehyde is hydrogenated to produce 4-acetoxybutanol, which then is dehydroacetoxylated to produce THF. The hydrogenation to produce 4-acetoxybutanol is preferably conducted according to the conditions described above. The 4-acetoxybutanol can then undergo a dehydroacetoxylation reaction to produce THF and acetic acid. The dehydroacetoxylation step is preferably performed at temperatures in the range of from 20 to 300° C. in the presence of a dehydroacetoxylation catalyst, such as silica, silica-alumina, and/or tungsten oxide. A final hydrolysis step may be performed to convert any 3-acetoxy-2-methylpropanol, formed by the hydrogenation of 3-acetoxy-2-methylpropionaldehyde, to 2-methyl-1,3-propanediol (MPD)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124805B2
Source datasetuspto-grants-2012_02
ORD IDord-cbdb500bbfb1456a850aae25c2b6b105
Source noteuspto-grants-2012_02