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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638577Generated: October 30, 2026

Water → 4-allyloxy-3-methyl-5,6,7,8-tetrahydroquinoline-N-oxide

https://huagongshe.com/reaction/1638577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAllyl AlcoholHCID 7858—
ReactantSodium HydroxideHCID 14798—
Reactant3-methyl-4-nitro-5,6,7,8-tetrahydroquinoline-N-oxideHCID 13960261—
Product4-allyloxy-3-methyl-5,6,7,8-tetrahydroquinoline-N-oxideHCID 14155520—

Reaction Steps

2.0 Grams of 3-methyl-4-nitro-5,6,7,8tetrahydroquinoline-N-oxide was dissolved in allyl alcohol. Then 0.6 g of sodium hydroxide was added thereto, and the mixture was stirred at 70°-80° C. for 3 hours. After the reaction was completed, the reaction mixture was concentrated under reduced pressure, to the residue thus obtained was added water, and was extracted with chloroform. The chloroform layer was washed with an aqueous solution saturated with sodium chloride, then dried with anhydrous magnsium sulfate. Chloroform was removed by evaporation under reduced pressure to obtain 1.4 g of 4-allyloxy-3-methyl-5,6,7,8-tetrahydroquinoline-N-oxide in the form of brown oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880815
Source datasetuspto-grants-1989_11
ORD IDord-22176e2832704fe880ec6c6d19284215
Source noteuspto-grants-1989_11