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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804450Generated: October 31, 2026

Pyridine → HCID 58374105, compound

https://huagongshe.com/reaction/1804450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantCyanuric fluorideHCID 12664—
ReactantHCID 58374151HCID 58374151—
SolventDichloromethaneHCID 6344—
ProductHCID 58374105HCID 58374105100.3%

Reaction Steps

To a mixture of 5-phenyl-4-(trifluoromethyl)isoxazole-3-carboxylic acid (197 mg, 0.766 mmol) and pyridine (0.074 mL, 0.919 mmol) in dichloromethane (5 mL) at room temperature was added cyanuric fluoride (0.078 mL, 0.919 mmol). The reaction mixture was stirred at room temperature for 18 h. The mixture was diluted with dichloromethane (40 mL) and washed with an ice-cold 0.5N aqueous solution of hydrochloric acid (20 mL). The aqueous layer was extracted with dichloromethane (20 mL), and the combined organic layers were washed with ice-cold water (20 mL) and dried over anhydrous magnesium sulfate. Concentration under reduced pressure afforded 5-phenyl-4-(trifluoromethyl)isoxazole-3-carbonyl fluoride (199 mg, 0.768 mmol, 100% yield) as a pale yellow oil. The compound had an HPLC retention time=2.53 min. (methyl ester)−Column: CHROMOLITH® SpeedROD 4.6×50 mm (4 min.); Solvent A=10% MeOH, 90% H2O, 0.1% TFA; Solvent B=90% MeOH, 10% H2O, 0.1% TFA.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354398B2
Source datasetuspto-grants-2013_01
ORD IDord-2d671eebe5954ac1a3ccd659f5301165
Source noteuspto-grants-2013_01