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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1646429Erstellt: 25. Oktober 2026

Ethanol → Ethyl 3-(4-chlorophenyl)-2,2-dimethylpropanoate

https://huagongshe.com/reaction/1646429

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktHexaneHCID 8058—
EduktHydrofluoric AcidHCID 14917—
EduktBenzenemethanol, 4-chloro-alpha-(1-methylethyl)-HCID 202426—
EduktHCID 178418416HCID 178418416—
KatalysatorHastelloy CHCID 11332432—
ProduktEthyl 3-(4-chlorophenyl)-2,2-dimethylpropanoateHCID 12373578—

Reaktionsbedingungen

Temperatur-30 °C

Reaktionsschritte

1-(4'-Chlorophenyl)-2-methyl-1-propanol (9.6 grams, 0.05 moles), ethanol (4.5 grams, 0.1 mole), and hexane (32 grams) are charged into a 300 cubic centimeter Hastelloy C autoclave. The autoclave is purged twice with nitrogen, evacuated to 100 mm Hg, and cooled to -30° C. Hydrogen fluoride (75 grams, 3.25 mole) is then added and the reactor is pressurized to 600 psig with carbon monoxide. The reaction mass is stirred for about an hour at room temperature. The hydrogen fluoride is vented and the contents are removed and poured onto crushed ice. A solution of 45% potassium hydroxide is added to the mixture until the pH of the mixture is adjusted to 6.0-6.5. The mixture is then extracted with ethyl acetate (3 times with 150 ml of ethyl acetate each time). The combined organic extract is dried with anhydrous magnesium sulfate, filtered, and concentrated to yield the crude product. The crude product is distilled under vacuum to give pure ethyl 2,2-dimethyl-3-(4'-chlorophenyl)propanoate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05179229
Quelldatensatzuspto-grants-1993_01
ORD IDord-4b0dbf58f1b3417681ace3e3d80539f9
Quellennotizuspto-grants-1993_01