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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 260651Erstellt: 26. Oktober 2026

Diisopropylamine → 3-Phenyl-2-t-butylcarboxymethylpropionic acid, ethyl ester

https://huagongshe.com/reaction/260651

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
EduktEthyl 3-phenylpropionateHCID 16237—
Edukttert-Butyl bromoacetateHCID 79177—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt3-Phenyl-2-t-butylcarboxymethylpropionic acid, ethyl esterHCID 8674901246%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Dissolve diisopropylamine (3.5 mL, 25 mmol) in tetrahydrofuran (30 mL). Add n-butyllithium (14 mL of a 1.6M solution in hexane, 22.4 mmol). Stir for 15 minutes and cool to -78° C. Add, by dropwise addition, ethyl dihydrocinnamate (3.5 mL, 20 mmol) and stir for 30 minutes. Add t-butyl bromoacetate (4.0 mL, 25 mmol) and gradually warm to room temperature overnight. Quench the solution with ammonium chloride solution (10 mL) and partition between water (25 mL) and ethyl ether (50 mL). Separate the organic phase, dry (MgSO4) and evaporate the solvent in vacuo. Purify by silica gel chromatography (5% ethyl acetate/hexane) to give 3-phenyl-2-t-butylcarboxymethylpropionic acid, ethyl ester as a pale yellow oil (2.68 g, 46%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05529997
Quelldatensatzuspto-grants-1996_06
ORD IDord-c28dd0fd4efe467bb54bfbf4c7b8e4bf
Quellennotizuspto-grants-1996_06