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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240583Generated: October 31, 2026

Trifluoroacetic anhydride → 7-(Benzyloxy)-[1,2,4]triazolo[1,5-a]pyridine

https://huagongshe.com/reaction/240583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 178526368HCID 178526368—
SolventTetrahydrofuranHCID 8028—
Product7-(Benzyloxy)-[1,2,4]triazolo[1,5-a]pyridineHCID 66937106—

Reaction Conditions

Temperature0 °C

Reaction Steps

Trifluoroacetic anhydride (2.62 mL, 18.9 mmol) was added dropwise to a solution of (Z)-N′-(4-(benzyloxy)pyridin-2-yl)-N-hydroxyformamidine (4.37 g, 17.9 mmol) in THF (180 mL), and the mixture was cooled to 0° C. The ice bath was then removed and the reaction was stirred for 12 hours. The reaction was concentrated to about 15-25 mL, then poured into 400 mL of iced 1 M NaOH. The mixture was stirred for 1 hour. The resulting white solids were collected by filtration, washed with hexanes, and dried under high vacuum for 1 hour to provide the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648087B2
Source datasetuspto-grants-2014_02
ORD IDord-78a748461afe482eb8b15c8e274cc96e
Source noteuspto-grants-2014_02