Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 430460Erstellt: 24. Oktober 2026

Ethyl Acetate → Ethyl 2-hydroxy-4-methyl-2-(trifluoromethyl)pent-4-enoate

https://huagongshe.com/de/reaction/430460

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktAmmonium ChlorideHCID 25517—
Edukt3-Bromo-2-methyl-1-propeneHCID 357785—
EduktEthyl 3,3,3-trifluoro-2-oxopropanoateHCID 2737239—
KatalysatorManganeseHCID 23930—
KatalysatorZincchlorideHCID 3007855—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 2-hydroxy-4-methyl-2-(trifluoromethyl)pent-4-enoateHCID 17935595—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

1.3 g of anhydrous zinc chloride and 13.2 g of granular manganese are heated to boiling in 100 ml of tetrahydrofuran and boiled with 0.2 ml of methallyl bromide for 30 minutes. Then, the solution of 25 g of methallylbromide and 17 g of trifluoropyruvic acid ethyl ester in 80 ml of tetrahydrofuran is added in drops at boiling heat over two hours and boiled for another hour. Then, it is added to saturated ammonium chloride solution and 300 ml of ethyl acetate while being cooled with ice, stirred for 30 minutes at 0° C., and the separated ethyl acetate phase is washed with saturated ammonium chloride solution and three times with water. The solvent is dried (Na2SO4) and concentrated by evaporation, and the residue is distilled in a vacuum. 17.6 g of 2-hydroxy-4-methylene-2-trifluoromethyl-valeric acid ethyl ester, boiling point 48° C., 1 hPa, is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06323199B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-605ea9751b734934af7fb3bb1d09a996
Quellennotizuspto-grants-2001_11