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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657207Generated: October 25, 2026

Methanol → Butanoic acid, 4-chloro-3-hydroxy-, ethyl ester

https://huagongshe.com/reaction/1657207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDimethyl SulfideHCID 1068—
ReactantEthyl AcetateHCID 8857—
ReactantOzoneHCID 24823—
Reactant(+)-2,2-Dimethyl-(3-chloro-2-hydroxypropyl)-1,3-dioxin-4-oneHCID 19096633—
ProductButanoic acid, 4-chloro-3-hydroxy-, ethyl esterHCID 437770466%

Reaction Conditions

Temperature80 °C

Reaction Steps

Ozone was introduced into a mixture of 225.5 mg (1 mmol) of (+)-2,2-dimethyl-(3-chloro-2-hydroxypropyl)-1,3-dioxin-4-one (96% ee) obtained in Example 4 and 20 ml of methanol at -78° C. for 5 hours, and 2 ml of dimethyl sulfide were added thereto, followed by stirring at the same temperature for 2 hours. The temperature was gradually returned to room temperature, and the solution was then stirred for 5 hours. Afterward, the solvent was distilled off, and the resultant residue was then dissolved in ethanol. 3 drops of concentrated sulfuric acid were added thereto, and the solution was then heated at 80° C. for 30 minutes. Next, ethanol was distilled off, and the residue was diluted with water. The solution was extracted with dichloromethane and then dried over anhydrous sodium sulfate, and the solvent was distilled off and the residue was then subjected to column chromatography (an eluent of hexane:ethyl acetate=5:1), thereby obtaining 109.4 mg (yield 66%) of (+)-ethyl 4-chloro-3-hydroxybutanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256800
Source datasetuspto-grants-1993_10
ORD IDord-aedc60aaefcb4224adf95a517fc2606f
Source noteuspto-grants-1993_10