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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330071Generated: October 30, 2026

Hydrochloric Acid → 3-Benzyl-5,6,7,8-tetrahydroquinoxalin-2(1H)-one

https://huagongshe.com/reaction/330071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,2-CyclohexanedioneHCID 13006—
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
ReactantPhenylalanine amide hydrochlorideHCID 11953719—
SolventMethanolHCID 887—
Product3-Benzyl-5,6,7,8-tetrahydroquinoxalin-2(1H)-oneHCID 17851734082.1%

Reaction Steps

A methanol (30 ml) solution of cyclohexane-1,2-dione (13.44 g, 0.12M) was added to phenylalanineamide hydrochloride (20.05 g, 0.1M) dissolved in methanol (200 ml) with cooling below -30° C., and aqueous 12.5N-NaOH (20 ml) was added dropwise thereto. The reaction mixture was stirred at below -30° C. for 30 minutes and was further stirred at room temperature for 3 hours. Conc. hydrochloric acid (25 ml) was added to the reaction mixture, and sodium bicarbonate (15 g) was added after 10 minutes stirring, the solvent then being distilled off in vacuo. The residue, to which was added water, was extracted three times with chloroform, and the extract was dried with anhydrous magnesium sulfate and concentrated in vacuo. The residue was recrystallized from acetone to obtain the product. (19.7 g, yield: 82.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04894453
Source datasetuspto-grants-1990_01
ORD IDord-72db7c37bcbc4fa48068c74312bc73c5
Source noteuspto-grants-1990_01