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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249781Generated: October 26, 2026

Acetaldehyde → 2-(1-hydroxyethyl)-3-hydroxy-6-methyl-pyran-4(1H)-one

https://huagongshe.com/reaction/1249781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
Reactant4H-Pyran-4-one, 5-hydroxy-2-methyl-HCID 69521—
SolventWaterHCID 962—
Product2-(1-hydroxyethyl)-3-hydroxy-6-methyl-pyran-4(1H)-oneHCID 1079722883%

Reaction Steps

Allomaltol (12.6 g, 100 mmol, 1 eq.) was added to 100 ml water and the pH of the solution was adjusted to 10.5 using 50% aqueous sodium hydroxides. Acetaldehyde (5.5 g, 125 mmol, 1.25 eq.) dissolved in 25 ml water was slowly added dropwise over 1 hour and the solution allowed to stir overnight. After adjustment to pH 1 with 37% hydrochloric acid, the reaction mixture was extracted with 3×150 ml of dichloromethane. The combined organic extracts were dried over anhydrous sodium sulphate, filtered and concentrated to yield the crude product. Recrystallisation from toluene afforded the pure product (14.1 g, 83%) as white needles. m.p. 127-130° C. [lit. 126-128° C.]. Ellis (1993)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06335353B1
Source datasetuspto-grants-2002_01
ORD IDord-7122cd02109f4645bcf99a051f9e8f7e
Source noteuspto-grants-2002_01