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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyraldehyde, cyclic acetal with glycerolHCID 347826—
Reactant[(2R,4R)-2-Propyl-1,3-dioxolan-4-yl]methanolHCID 12627409—
CatalystPalladiumHCID 23938—
SolventGlycerolHCID 753—
Product3-Butoxy-1,2-propanediolHCID 263027—

Reaction Conditions

Temperature200 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388105B2
Source datasetuspto-grants-2016_07
ORD IDord-2b61818519914cdeb27fa7406b072f44
Source noteuspto-grants-2016_07