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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818930Generated: October 31, 2026

Dichloromethane → Difluoro-[4-(3-trifluoromethyl-benzoylamino)-phenyl]-acetic acid ethyl ester

https://huagongshe.com/reaction/1818930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 2,2-difluoro-2-(4-nitrophenyl)acetateHCID 10586437—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductDifluoro-[4-(3-trifluoromethyl-benzoylamino)-phenyl]-acetic acid ethyl esterHCID 68422864—

Reaction Steps

Difluoro-(4-nitro-phenyl)-acetic acid ethyl ester (compound 32.1) is reacted according to Sato, K. et. al. Chem. Pharm. Bull. 1999, 47, 1013). Briefly, compound 32.1 and catalytic Pd/C in EtOAc are placed under an atmosphere of hydrogen for 3 hours. The reaction mixture is filtered, concentrated and taken on crude to the next reaction. The crude compound, dichloromethane, 3-(trifluoromethyl)benzoyl chloride and DIEA are stirred at room temperature for 10 minutes. Water is added after which the mixture partitioned between EtOAc and water. The organic layer is separated, washed with brine, dried, filtered and concentrated under reduced pressure. Purification by flash column chromatography on silica gel using a gradient of EtOAc/hexanes provides difluoro-[4-(3-trifluoromethyl-benzoylamino)-phenyl]-acetic acid ethyl ester (compound 32.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601725B2
Source datasetuspto-grants-2009_10
ORD IDord-09cc051c8560489eba71c29024446eb6
Source noteuspto-grants-2009_10