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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638578Generated: November 4, 2026

Acetic Anhydride → 8-Acetoxy-4-allyloxy-3-methyl-5,6,7,8-tetrahydroquinoline

https://huagongshe.com/reaction/1638578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-allyloxy-3-methyl-5,6,7,8-tetrahydroquinoline-N-oxideHCID 14155520—
SolventWaterHCID 962—
Product8-Acetoxy-4-allyloxy-3-methyl-5,6,7,8-tetrahydroquinolineHCID 14155521—

Reaction Conditions

Temperature90 °C

Reaction Steps

To 4.8 g of 4-allyloxy-3-methyl-5,6,7,8-tetrahydroquinoline-N-oxide was added 50 ml of acetic anhydride, and the mixture was stirred at 90° C. for 5 hours. After the reaction was completed, acetic anhydride was removed by evaporation under reduced pressure, to the residue thus obtained was added water and then extracted with chloroform. The chloroform layer was washed with an aqueous solution of sodium hydroxide and an aqueous solution saturated with sodium chloride, then dried with anhydrous magnesium sulfate. Chloroform was removed by evaporation under reduced pressure to obtain 5.0 g of 8-acetoxy-4-allyloxy-3-methyl-5,6,7,8-tetrahydroquinoline in the form of brown oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880815
Source datasetuspto-grants-1989_11
ORD IDord-868c3e11c46245968f1bc57f73633de2
Source noteuspto-grants-1989_11