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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256465Generated: October 31, 2026

Methanol → 1,3-Diisobutyryloxyacetone

https://huagongshe.com/reaction/2256465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPyridineHCID 1049—
ReactantIsobutyric anhydrideHCID 7346—
Reactant1,1-Dihydroxypropan-2-oneHCID 13180982—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl AcetateHCID 8857—
Product1,3-DiisobutyryloxyacetoneHCID 15521806—

Reaction Steps

A 100 ml reaction vessel was charged with 4.18 g of dihydroxyacetone (monomer), 11.2 ml of pyridine and 10 mg of 4-dimethylaminopyridine and the mixture was stirred at room temperature. Thereto was added dropwise 16.7 ml of isobutyric anhydride over 30 minutes. After the dropping, the resulting liquid was further stirred for 1 hour and then 1 ml of methanol was added thereto and the resulting liquid was further stirred for 1 hour. To the reaction mixture was added ethyl acetate and the organic layer was separated. The organic layer was washed with water and further washed with saturated aqueous solution with sodium bicarbonate and 1N HCl. Then, the solvent was removed under reduced pressure. The residue was distilled under reduced pressure to give 7.47 g of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654472
Source datasetuspto-grants-1997_08
ORD IDord-6a9e53dc93834de88a3f203d8a25ae6a
Source noteuspto-grants-1997_08