Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907599Generated: October 31, 2026

Trifluoroacetic acid → 2-Amino-3,6-dimethoxyquinoxaline

https://huagongshe.com/reaction/1907599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3,6-Dimethoxy-2-(2,4-dimethoxybenzylamino)quinoxalineHCID 69242572—
SolventDichloromethaneHCID 6344—
Product2-Amino-3,6-dimethoxyquinoxalineHCID 6924521395.2%

Reaction Steps

To 3,6-dimethoxy-2-(2,4-dimethoxybenzylamino)quinoxaline (4.45 g, 12.8 mmol), 70 ml of 50% trifluoroacetic acid in dichloromethane was added at room temperature. The resulting mixture was stirred at room temperature for 18 hours and concentrated under the reduced pressure to remove the solvent. The residue was neutralized with saturated sodium bicarbonate solution and then NaCl solution was added thereto. The product was extracted with dichloromethane and the organic layer was dried over MgSO4. After concentration under the reduced pressure, the crude product was purified by SiO2 column chromatography. Extraction of the residue with a n-hexane:ethyl acetate mixture and concentration gave 2.50 g of the titled compound (yield, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598173B2
Source datasetuspto-grants-2013_12
ORD IDord-3b52ecada5c741c08b7e6e1d6a109ac5
Source noteuspto-grants-2013_12