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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857988Generated: November 1, 2026

Acetic Anhydride → HCID 22648244, compound

https://huagongshe.com/reaction/857988

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 numberUS07148232B2
Source datasetuspto-grants-2006_12
ORD IDord-de8c98e2b4c74f6dba47d2e18364f2e9
Source noteuspto-grants-2006_12