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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441221Generated: October 29, 2026

HCID 22405140, compound → 168045-49-6

https://huagongshe.com/reaction/441221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22405140HCID 22405140—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product168045-49-6HCID 1068325516.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of N-ethoxycarbonylmethyl-N-(4-nitrobenzoyl)-2-nitroaniline (500 mg) and iron powder (374 mg) in a mixture of ethanol (10 ml) and acetic acid (1 ml) was heated at 80° C. for 3 hours and the solution was cooled to ambient temperature. The mixture was filtered through celite and the filtrate was evaporated in vacuo. The residue was dissolved in chloroform (20 ml) and the solution was neutralized with aqueous sodium hydrogen carbonate. The solution was filtered through celite and the organic filtrate was washed with brine. The solution was dried over magnesium sulfate and the solvent was evaporated in vacuo to give a crude oil. The oil was purified by silica gel column (10 g, 2% methanol in chloroform) to give 4-(4-aminobenzoyl)-1,2,3,4-tetrahydroquinoxalin-2-one (58 mg) as a pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521170
Source datasetuspto-grants-1996_05
ORD IDord-d0beeaae02404aa3ae474cbcc801bf1b
Source noteuspto-grants-1996_05