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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1646160Erstellt: 26. Oktober 2026

Iodine → 4-Acetoxy-4-methyl-3-pentyl-tetrahydrofuran-2-one

https://huagongshe.com/reaction/1646160

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktTolueneHCID 1140—
EduktAcetoxyacetoneHCID 11593—
EduktEthyl 2-bromoheptanoateHCID 95333—
KatalysatorZincHCID 23994—
Produkt4-Acetoxy-4-methyl-3-pentyl-tetrahydrofuran-2-oneHCID 1980157743,5%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Zinc powder (65.37 g, 1 mol) and 3.27 g (50 mmol) of iodine are placed in 400 ml of toluene. This violet suspension is heated to 80° C. in an oil bath while stirring and treated within 80 minutes with a solution of 118.55 g (500 mmol) of ethyl 2-bromoheptanoate and 87.08 g (750 mmol) of acetoxyacetone in 100 ml of toluene. The exothermic reaction which sets in immediately can be held at 80°-90° C. by removing the oil bath. After a further 90 minutes at 80° C. the reaction mixture, cooled to room temperature, is treated with 400 ml of ice-water and then with 120 ml of 20% HCl and stirred for 30 minutes. Then, it is extracted three times with 500 ml of ether in a separating funnel. The ether phases are washed with 500 ml of sat. NaHCO3 solution and with 500 ml of sat. NaCl solution, dried over MgSO4 and concentrated on a rotary evaporator. The crude product distills at 110°-112° C./0.06 mbar and gives 49.64 g (43.5%) of 4-acetoxy-4-methyl-3-pentyl-tetrahydrofuran-2-one.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05179077
Quelldatensatzuspto-grants-1993_01
ORD IDord-bba38ad218eb427bbc5ed3f276cebf29
Quellennotizuspto-grants-1993_01