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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838824Generated: November 2, 2026

Acetic Anhydride → HCID 22648244, compound

https://huagongshe.com/reaction/1838824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178507989HCID 178507989—
SolventWaterHCID 962—
ProductHCID 22648244HCID 22648244—

Reaction Steps

3-Aminoquinolin-4-ol (6 g) was refluxed with acetic anhydride (8 eq.) until analysis by thin layer chromatography indicated that the reaction was complete. The reaction mixture was cooled, diluted with ice and water, made basic with 10% sodium hydroxide and then extracted with dichloromethane. The extract was washed with water and brine, dried over magnesium sulfate and then concentrated under vacuum. The residue was purified by column chromatography (silica gel eluting with methanol/ethyl acetate) to provide 5.1 g of 2-methyloxazolo[4,5-c]quinoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677334B2
Source datasetuspto-grants-2004_01
ORD IDord-8128f9d013b6431ebd2b11c1364289b0
Source noteuspto-grants-2004_01