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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238172Erstellt: 24. Oktober 2026

Water → Tert-butyl 3-methyl-2-(4-methylphenyl)pentanoate

https://huagongshe.com/de/reaction/238172

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt2-BromobutaneHCID 6554—
Edukttert-Butyl (4-methylphenyl)acetateHCID 12362014—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDimethylformamideHCID 6228—
ProduktTert-butyl 3-methyl-2-(4-methylphenyl)pentanoateHCID 58074556—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Under argon, 19.58 g (174.5 mmol) of potassium tert-butoxide were initially charged in 200 ml of DMF, the mixture was cooled to 0° C., 30 g (145.4 mmol) of tert-butyl (4-methylphenyl)acetate, dissolved in 50 ml of DMF, were added slowly and the mixture was then stirred at 0° C. for 30 min. 18.95 ml (174.5 mmol) of 2-bromobutane were then slowly added drowise, and the solution was stirred at 0° C. for 4 h. 200 ml of water and 200 ml of diethyl ether were then added to the reaction solution. The aqueous phase was extracted twice with diethyl ether. The combined organic phases were dried over magnesium sulfate. After filtration, the solvent was removed under reduced pressure. The crude product was purified chromatographically on silica gel (mobile phase cyclohexane/ethyl acetate 20:1). This gave 15.5 g (59.1 mmol, 40.6% of theory) of a colorless liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642592B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-d849c72962184e80be70b139d94a6ff1
Quellennotizuspto-grants-2014_02