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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441452Generated: November 1, 2026

Trichloroacetyl chloride → 2,2,2-trichloro-N-[2-(3-chlorobenzoyl)-4-(4-fluorobenzoyl)phenyl]-acetamide

https://huagongshe.com/reaction/1441452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl chlorideHCID 6420—
ReactantTriethylamineHCID 8471—
Reactant[2-Amino-5-(4-fluorobenzoyl)phenyl](3-chlorophenyl)-methanoneHCID 17976107—
SolventDichloromethaneHCID 6344—
Product2,2,2-trichloro-N-[2-(3-chlorobenzoyl)-4-(4-fluorobenzoyl)phenyl]-acetamideHCID 6868885495.5%

Reaction Conditions

Temperature5 °C

Reaction Steps

Trichloro-acetylchloride (0.0848 mol) was added dropwise at 5° C. to a mixture of intermediate 3 (0.0707 mol) in DCM (250 ml) under N2 flow. The mixture was stirred at 5° C. for 30 minutes. Triethylamine (0.0848 mol) was added dropwise at 5° C. The mixture was stirred at 5° C. for 1 hour, then at room temperature for 2 hours and poured out into ice water. DCM was added. The mixture was extracted with DCM. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated. The residue was crystallized from diethyl ether/DIPE. The precipitate was filtered off and dried, yielding 33.7 g (95%) of 2,2,2-trichloro-N-[2-(3-chlorobenzoyl)-4-(4-fluorobenzoyl)phenyl]-acetamide (intermediate 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655654B2
Source datasetuspto-grants-2010_02
ORD IDord-65b5028dfd554e3f9d1dba402b98769a
Source noteuspto-grants-2010_02