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HRID 486848Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/486848

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktDimethyl SulfideHCID 1068—
EduktEthyl AcetateHCID 8857—
EduktOzoneHCID 24823—
Edukt(+)-2,2-Dimethyl-(3-chloro-2-hydroxypropyl)-1,3-dioxin-4-oneHCID 19096633—
ProduktButanoic acid, 4-chloro-3-hydroxy-, ethyl esterHCID 437770466%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05292891
Quelldatensatzuspto-grants-1994_03
ORD IDord-d4141169b3a64ab4b95d97dc751e2fd7
Quellennotizuspto-grants-1994_03