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HRID 595792Erstellt: 26. Oktober 2026

Ethyl Acetate → (+/-)-(3-Fluoro-4-((2,2,2-trifluoro-1-phenylethyl)carbamoyl)phenyl)boronic acid

https://huagongshe.com/reaction/595792

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Eduktalpha-(Trifluoromethyl)benzenemethanamineHCID 89166—
Edukt4-Carboxy-3-fluorophenylboronic acidHCID 2763201—
EduktHCID 15569623HCID 15569623—
LösungsmittelDichloromethaneHCID 6344—
Produkt(+/-)-(3-Fluoro-4-((2,2,2-trifluoro-1-phenylethyl)carbamoyl)phenyl)boronic acidHCID 123606597—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A mixture of 4-borono-2-fluorobenzoic acid (54 mg, 0.294 mmol) in DCM (1468 μL) was cooled to 0° C. Then ghosez reagent N,N,3-trimethylbut-2-en-2-amine (65.8 μL, 0.587 mmol) was added and the whole mixture was stirred at rt for 20 min. The mixture was added into a mixture of TEA (246 μL, 1.762 mmol), 2,2,2-trifluoro-1-phenylethanamine (59.1 mg, 0.338 mmol) and DCM (1468 μL). The reaction was stirred at room temperature for 2 h. To the reaction mixture was added EtOAc, and washed with sat. sodium bicarbonate, water, and dried over Na2SO4. Filtered and concentrated to provide the crude product which was taken to the next step without further purification. LCMS (m/z): 342.2 (MH+), 0.84 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09242996B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-49a1d99c282d4e52924273ca614f866f
Quellennotizuspto-grants-2016_01