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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430551Generated: October 31, 2026

Acetic Anhydride → HCID 22648244, compound

https://huagongshe.com/reaction/430551

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 numberUS06323200B1
Source datasetuspto-grants-2001_11
ORD IDord-0843e10bee2d4b94a002d1a1a3646bf5
Source noteuspto-grants-2001_11