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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 32871Erstellt: 25. Oktober 2026

Toluene → 2-Acetylamino-3,3-bis(4-fluorophenyl)propanoic acid

https://huagongshe.com/reaction/32871

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktAcetamidomalonic acid diethyl esterHCID 14041—
EduktSodium hydrideHCID 24758—
EduktHCID 23154741HCID 23154741—
LösungsmittelWaterHCID 962—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt2-Acetylamino-3,3-bis(4-fluorophenyl)propanoic acidHCID 1197782976,2%

Reaktionsschritte

To a solution of diethyl acetamidomalonate (1.09 g, 5 mmol) in N-methyl-2-pyrrolidone (4 mL) was added 55% sodium hydride (219 mg, 5 mmol), and the mixture was stirred at room temperature for 1 hr. Bis(4-fluorophenyl)methylene bromide (990 mg, 4 mmol) was added, and the mixture was stirred at 50° C. for 4 hrs. After completion of the reaction, toluene (20 mL) and water (10 mL) were added to the reaction mixture and the mixture was partitioned. The obtained organic layer was washed twice with water (10 mL) and concentrated. Ethanol (4.5 mL) and 2M aqueous sodium hydroxide solution (5 mL) were added to the concentrated solution, and the mixture was stirred at 90° C. for 16 hrs. The reaction mixture was allowed to cool to 25° C., toluene (8 mL) and water (5 mL) were added, and the mixture was partitioned. The aqueous layer was concentrated to a half volume, and isopropyl acetate (8 mL) and water (10 mL) were added. The mixture was adjusted to pH 1.1 with concentrated hydrochloric acid and partitioned. The organic layer was washed with water (10 mL), concentrated and dried under vacuum to give the title compound (973 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07427688B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-4bb52830e22a47a1a7957e48c82aa349
Quellennotizuspto-grants-2008_09