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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227366Generated: October 27, 2026

Water → 8,9-Dimethoxychromeno[4,3,2-de]isoquinoline

https://huagongshe.com/reaction/2227366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-Dimethoxy-6-(5-nitroisoquinolin-4-yl)phenolHCID 12971920—
SolventDimethylformamideHCID 6228—
Product8,9-Dimethoxychromeno[4,3,2-de]isoquinolineHCID 12971921—

Reaction Conditions

Temperature80 °C

Reaction Steps

Phenol 5 (4.65 g, 0.014 mol) was dissolved in 100 ml of dry N,N-dimethylformamide. The solution was degassed with argon for thirty minutes. Potassium carbonate (5.80 g, 0.042 mol) was added to the yellow solution in one portion. After heating at 80° C. for one hour, the mixture had turned brown and no more starting material remained. After the solution was cooled to room temperature, 200 ml of water was added. The aqueous layer was extracted with dichloromethane (3×500 ml), this organic extract was washed with water (3×500 ml), dried (Na2SO4), and concentrated. A white powder (3.65 g 92%) was obtained that was used in the next reaction without further purification. An analytical sample was recrystallized from ethyl acetate:hexane: mp 195-196° C.; 1H NMR: (300 MHz, CDCl3): 9.02 (s, 1H); 8.82 (s, 1H); 7.87 (d, 1H, J=8.7 Hz); 7.62 (m, 3H); 7.32 (dd, 1H, J=6.0, 1.5 Hz); 6.95 (d, J=9.6 Hz); 3.88 (s, 3H); 3.82 (s, 3H). CIMS m/z: 280 (M+H+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413977B1
Source datasetuspto-grants-2002_07
ORD IDord-5a8d628231694b96bedf759081e7cb3f
Source noteuspto-grants-2002_07