Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352607Generated: October 29, 2026

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

https://huagongshe.com/reaction/2352607

Reaction equation

Participants

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

Reaction Conditions

Temperature-30 °C

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04877875
Source datasetuspto-grants-1989_10
ORD IDord-7f4030c7e32346898a864188fea944aa
Source noteuspto-grants-1989_10