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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1424412Erstellt: 26. Oktober 2026

Oxalyl chloride → 2-(2-Bromo-2-(4-fluorophenyl)acetamido)-4-fluorobenzamide

https://huagongshe.com/reaction/1424412

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
Edukt2-Amino-4-fluorobenzamideHCID 10241004—
EduktBromo(4-fluorophenyl)acetic acidHCID 16217752—
LösungsmittelPyridineHCID 1049—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(2-Bromo-2-(4-fluorophenyl)acetamido)-4-fluorobenzamideHCID 66610889—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 2-bromo-2-(4-fluorophenyl)acetic acid (425 mg, 1.82 mmol) in DCM (5 mL) and DMF (0.05 mL) was added oxalyl chloride (0.17 mL, 1.91 mmol) and the solution was stirred for 0.75 h. The solution was then cooled to 0° C. and a solution of 2-amino-4-fluorobenzamide (267 mg, 1.73 mmol) in pyridine (1 mL) was added. The solution was stirred at rt for 1 h and then evaporated. The crude residue was partitioned between EtOAc and 2 N HCl. The EtOAc layer was evaporated to give 2-(2-bromo-2-(4-fluorophenyl)acetamido)-4-fluorobenzamide as a crude oil which was used without further purification. (420 mg, 62%). LC-MS (ESI) m/z 369 (M−H)−.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08927711B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-c1c9c5d38bb246cb9635ed326c961b2a
Quellennotizuspto-grants-2015_01