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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424412Generated: October 25, 2026

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

https://huagongshe.com/reaction/1424412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-Amino-4-fluorobenzamideHCID 10241004—
ReactantBromo(4-fluorophenyl)acetic acidHCID 16217752—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-(2-Bromo-2-(4-fluorophenyl)acetamido)-4-fluorobenzamideHCID 66610889—

Reaction Conditions

Temperature0 °C

Reaction Steps

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)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927711B2
Source datasetuspto-grants-2015_01
ORD IDord-c1c9c5d38bb246cb9635ed326c961b2a
Source noteuspto-grants-2015_01