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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1051392Erstellt: 26. Oktober 2026

Potassium Hydroxide → 4,4,4-Trifluoro-3-formyl-butyric acid ethyl ester

https://huagongshe.com/reaction/1051392

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
EduktEthyl 4,4,4-trifluoro-3-(nitromethyl)butanoateHCID 268363—
EduktPotassium PermanganateHCID 516875—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4,4,4-Trifluoro-3-formyl-butyric acid ethyl esterHCID 90103465—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

In a 100 mL round-bottomed flask, KOH (356 mg, 5.45 mmol) was combined with H2O (50 ml) to give a colorless solution and cooled to 0° C. 4,4,4-Trifluoro-3-nitromethyl-butyric acid ethyl ester (1.25 g, 5.45 mmol) in 10 ml THF was added and the resulting reaction mixture was stirred for 20 min. This was followed by addition of MgSO4 (657 mg, 5.45 mmol) in 5 ml of H2O then by KMnO4 (862 mg, 5.45 mmol) in 30 ml of H2O. The resulting reaction mixture was stirred for 30 min, filtered through celite and the celite cake washed with CH2Cl2. The combined filtrate and washes were washed with brine, dried over Na2SO4, filtered and concentrated to afford 4,4,4-trifluoro-3-formyl-butyric acid ethyl ester as a liquid which was used without purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09388172B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-955962637e704064a17b9764098c1f08
Quellennotizuspto-grants-2016_07