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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827354Generated: November 2, 2026

Water → HCID 69592463, compound

https://huagongshe.com/reaction/1827354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-3-(trifluoromethyl)anilineHCID 67574—
ProductHCID 22137855HCID 22137855—
ProductHCID 69592463HCID 695924639%

Reaction Conditions

Temperature70 °C

Reaction Steps

The required N-(4-chloro-3-trifluoromethylphenyl)glycine was prepared as follows. A mixture of 4-chloro-3-trifluoromethylaniline (1.369 g, 7 mmol), ethyl bromoacetate (1.55 mL, 14 mmol), K2CO3 (2.764 g, 20 mmol) in DMF (40 mL) was heated at 70° C. overnight. It was then poured into water and extracted with EtOAc. The organic layer was separated, washed with brine, dried with anhydrous Na2SO4, concentrated by rotary evaporation and purified by flash chromatography on silica gel with a gradient elution of 20–40% EtOAc/hexanes to afford ethyl N-(4-chloro-3-trifluoromethylphenyl)glycine as a white solid (0.180 g, 9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053234B2
Source datasetuspto-grants-2006_05
ORD IDord-3dd948c1453a4774b3434fdd0dff2cc3
Source noteuspto-grants-2006_05