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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872621Generated: October 31, 2026

Acetic Anhydride → HCID 22648244, compound

https://huagongshe.com/reaction/1872621

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 numberUS06110929
Source datasetuspto-grants-2000_08
ORD IDord-6e4b2ca2d9fe4e0f882d7bcd0675a64f
Source noteuspto-grants-2000_08