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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029408Generated: October 26, 2026

Acetic Anhydride → 1-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-1-ethanone

https://huagongshe.com/reaction/1029408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-Phenylpyrazolo[1,5-a]pyridineHCID 15620342—
CatalystSulfuric AcidHCID 1118—
SolventSodium HydroxideHCID 14798—
Product1-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-1-ethanoneHCID 1070495647.7%

Reaction Steps

2-Phenylpyrazolo[1,5-a]pyridine (2.00 g) was added to a stirred solution of acetic anhydride (4.20 g) and two drops of sulfuric acid at room temperature. After being stirred under reflux for 14 hours, the reaction mixture was poured onto 80 ml of 4 N NaOH aqueous solution and extracted with chloroform (30 ml×2). The extracts were combined and washed with water (30 ml), saturated sodium chloride aqueous solution (30 ml), then dried over magnesium sulfate and evaporated in vacuo. The residual crystals were recrystallized from diisopropyl ether to give 2-phenyl-3-acetylpyrazolo-[1,5-a]pyridine (1.16 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102878
Source datasetuspto-grants-1992_04
ORD IDord-822cc392bbe747b69933a295697522b0
Source noteuspto-grants-1992_04