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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880666Generated: October 31, 2026

Tetrahydrofuran → HCID 178517569, compound

https://huagongshe.com/reaction/1880666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 86647330HCID 86647330—
SolventWaterHCID 962—
ProductHCID 178517569HCID 178517569—

Reaction Steps

To 3 ml of tetrahydrofuran were added 0.3 g of 3-fluoro-4-trifluoromethylpyridine-2-carboxamide=oxime and 0.31 g of 1,1′-carbonyldiimidazole, and the mixture was stirred at room temperature for 2 hours. Thereafter, 0.29 g of 1,8-diazabicyclo[5,4,0]undec-7-ene was added, and the mixture was stirred for 4 hours. To the reaction solution were added water and a 10% aqueous HCl solution, the resultant solution was extracted with ethyl acetate three times, and the organic layers were combined, dried with anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.19 g of 3-(3-fluoro-4-trifluoromethylpyridin-2-yl)-1,2,4-oxadiazol-5-one (present compound (50)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318776B2
Source datasetuspto-grants-2012_11
ORD IDord-aa47defba3d940b29d574cf133b9febb
Source noteuspto-grants-2012_11