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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6872Erstellt: 23. Oktober 2026

Sodium Carbonate → N-cyclopropyl-3-(4,4-diethoxybutyl)-4-fluorobenzamide

https://huagongshe.com/de/reaction/6872

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt9-Borabicyclo(3.3.1)nonaneHCID 78966—
Edukt4,4-Diethoxybut-1-eneHCID 256426—
Edukt3-Bromo-N-cyclopropyl-4-fluorobenzamideHCID 22019090—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelBenzeneHCID 241—
LösungsmittelEthanolHCID 702—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-cyclopropyl-3-(4,4-diethoxybutyl)-4-fluorobenzamideHCID 2201916393,4%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A solution of 3-butenal diethyl acetal (144 mg, 1 mmol) and 9-BBN (0.5 M in THF, 2.2 mL, 1.1 mmol) was stirred at RT for 1 h. The mixture was concentrated and to the residue were added benzene (2 mL), EtOH (1 mL), aqueous Na2CO3 solution (2M, 1 mL), 3-bromo-4-fluoro-N-cyclopropylbenzamide (127 mg, 0.5 mmol) and Pd(Ph3P)4 (40 mg). The resulting mixture was stirred at 80° C. for 2 h. The mixture was then cooled to RT and diluted with ethyl acetate (10 mL) and washed with water. The organic layer was separated and concentrated. The residue was purified by column chromatography (SiO2; EtOAc/hexane 1:3) to afford N-cyclopropyl-3-(4,4-diethoxybutyl)-4-fluorobenzamide (151 mg, 93%). This material was dissolved in acetone (1 mL) and 3 N HCl solution (0.2 mL) and stirred at RT for 1 h. The mixture was neutralized with NaHCO3 solution and extracted with ethyl acetate (3×5 mL). The organic layer was dried and concentrated to afford N-cyclopropyl-4-fluoro-3-(4-oxo-butyl)-benzamide (110 mg, 94%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084160B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-b66a4138f5a24ea6bea939d006b10a7b
Quellennotizuspto-grants-2006_08