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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304909Generated: October 31, 2026

Ethanol → HCID 22962031, compound

https://huagongshe.com/reaction/2304909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethylamineHCID 6329—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant4'-(Trifluoromethyl)(1,1'-biphenyl)-2-carboxylic acidHCID 55251—
Reactant1-HydroxybenzotriazoleHCID 75771—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 22962031HCID 2296203181%

Reaction Conditions

Temperature0 °C

Reaction Steps

At 0° C. 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (7.2 g, 37.57 mmol) was added to a solution of 4′-(trifluoromethyl)-2-biphenylcarboxylic acid (10.0 g, 37.57 mmol) and 1-hydroxybenzotriazole ( 5.1 g, 37.57 mmol) in DMF (50 ml) and DCM (20 ml). The reaction mixture was stirred for 20 min at 0° C. An 8.3 M solution of methylamine in ethanol (94 ml, 751 mmol) was added. The reaction mixture was stirred for 16 hours, while it was warming up to room temperature. It was diluted with ethyl acetate (100 ml) and washed with a 10% aqueous solution of sodium hydrogen sulphate (100 ml). The aqueous phase was extracted with ethyl acetate (3×70 ml). The combined organic layers were washed with a saturated aqueous solution of sodium hydrogen carbonate (100 ml) and dried over magnesium sulphate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (200 g), using ethyl acetate/heptane (2:1) as eluent, to give 8.50 g of 4′-(trifluoromethyl)biphenyl-2-carboxylic acid methylamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437147B1
Source datasetuspto-grants-2002_08
ORD IDord-17c03cf083e24d9a9aeb6521f1a9062d
Source noteuspto-grants-2002_08