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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384432Generated: October 31, 2026

Acetic Anhydride → HCID 59527213, compound

https://huagongshe.com/reaction/384432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 59527026HCID 59527026—
ProductHCID 59527213HCID 59527213—

Reaction Steps

4-(Benzyloxy)-2,3,6-trimethylquinoline-1-oxide (1.18 g) was dissolved in acetic anhydride (32 mL), followed by stirring at room temperature for 2 hours. After the solvent was evaporated under reduced pressure, water (50 mL) was added to the residue, followed by extraction with ethyl acetate (100 mL). The organic layer was washed sequentially with water and saturated brine, and dried. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: chloroform) to obtain [4-(benzyloxy)-3,6-dimethylquinolin-2-yl]methyl acetate (1.25 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367702B2
Source datasetuspto-grants-2013_02
ORD IDord-77b0436e277e4311917f40b337ca5bf9
Source noteuspto-grants-2013_02