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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7805Generated: October 25, 2026

Triethylamine → HCID 178418902, compound

https://huagongshe.com/reaction/7805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Trifluoromethyl)benzoyl chlorideHCID 67607—
ReactantHCID 178418959HCID 178418959—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178418902HCID 17841890260%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-amino-5-bromopyridin-2-ol from Step C (1.5 g, 7.9 mol) and triethylamine (1.64 mL, 11.9 mol) in tetrahydrofuran (15.8 mL) at 0 C was added dropwise 4-trifluoromethylbenzoyl chloride (1.2 mL, 7.9 mol). The reaction mixture was stirred at 0° C. for 1 h and warmed to room temperature for 15 h. Potassium carbonate (1.64 g, 11.9 mol) and methanol (15.8 mL) were added and the reaction mixture was stirred at room temperature for 6 h. The reaction mixture was diluted with ethyl acetate (100 mL) and washed with saturated ammonium chloride solution and brine. The separated organic layer was dried with sodium sulfate, filtered and concentrated in vacuo. Purification by medium pressure liquid chromatography on silica gel (1:5 ethyl acetate/hexanes) gave 1.72 g (60%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087622B2
Source datasetuspto-grants-2006_08
ORD IDord-398716f2fe394a7f9a626f6e1dd67830
Source noteuspto-grants-2006_08