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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168758Generated: November 1, 2026

Acetic Anhydride → HCID 22648244, compound

https://huagongshe.com/reaction/1168758

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 numberUS06627638B2
Source datasetuspto-grants-2003_09
ORD IDord-04395587a92246369d4cbb587fe645f3
Source noteuspto-grants-2003_09