HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050892Generated: October 30, 2026
Butyraldehyde, cyclic acetal with glycerol → 3-Butoxy-1,2-propanediol
https://huagongshe.com/reaction/1050892
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butyraldehyde, cyclic acetal with glycerol | HCID 347826 | — |
| Reactant | [(2R,4R)-2-Propyl-1,3-dioxolan-4-yl]methanol | HCID 12627409 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Glycerol | HCID 753 | — |
| Product | 3-Butoxy-1,2-propanediol | HCID 263027 | — |
Reaction Steps
16.6 g of an equimolar mixture of cis/trans-4-hydroxymethyl-2-propyl-1,3-dioxolane and 5-hydroxy-2-propyl-1,3-dioxane were combined with 100 g of glycerin (glycerol) in a 300 mL stainless steel autoclave. 2.0 g of 5% Pd/C catalyst were added and the autoclave was sealed. The reactor was heated to 200° C. The reactor was then brought to an operating pressure of 6.89 MPa and stirring commenced at 750 rpm. Pressure was maintained through the duration of the experiment. After 2 h, the autoclave was cooled and remaining gas vented. The autoclave was opened, its contents filtered, and the filtrate analyzed by gas chromatography (GC). 76% conversion of the acetal mixture was observed. Upon analysis of the results, the mixture was found to demonstrate 26.1% selectivity to 2-butoxy-1,3-propanediol, 71.7% 3-butoxy-1,2-propanediol, and the balance n-butanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09388105B2 |
|---|
| Source dataset | uspto-grants-2016_07 |
|---|
| ORD ID | ord-2b61818519914cdeb27fa7406b072f44 |
|---|
| Source note | uspto-grants-2016_07 |
|---|