HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645463Generated: October 30, 2026
4-Acetoxybutyraldehyde → 4-Hydroxybutyl acetate
https://huagongshe.com/reaction/1645463
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Acetoxybutyraldehyde | HCID 11007927 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Hydroxybutyl acetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124805B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-cbdb500bbfb1456a850aae25c2b6b105 |
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| Source note | uspto-grants-2012_02 |
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