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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661830Generated: October 28, 2026

(1,1'-Biphenyl)-2-ol → 2-Quinoxalin-6-yl-malonic acid diethyl ester

https://huagongshe.com/reaction/1661830

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1,1'-Biphenyl)-2-olHCID 7017—
ReactantDiethyl MalonateHCID 7761—
ReactantCesium carbonateHCID 10796—
Reactant6-IodoquinoxalineHCID 24271765—
CatalystCopper iodideHCID 83717—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Quinoxalin-6-yl-malonic acid diethyl esterHCID 67427587—

Reaction Steps

A solution of 6-iodo-quinoxaline (0.323 g, 1.26 mmol), malonic acid diethyl ester (0.404 g, 2.52 mmol), copper iodide (0.012 g, 0.063 mmol), biphenyl-2-ol (0.021 g, 0.126 mmol) and cesium carbonate (0.616 g, 1.89 mmol) in THF (5 mL) was heated to 70° C. in a sealed tube for 24 hours. The solution was then cooled to room temperature, water was added and the crude product was extracted from ethyl acetate. The product was purified via silica gel column chromatography in hexane:ethyl acetate (1:1) to give 2-quinoxalin-6-yl-malonic acid diethyl ester. 2-quinoxalin-6-yl -malonic acid diethyl ester (0.066 g, 0.229 mmol) was added to a solution of sodium hydroxide [2N] (0.229 mL) in methanol (2 mL) and stirred for several hours at room temperature. The reaction was then evaporated in vacuo, 1N HCl was added and the product was extracted with ethyl acetate to give 0.030 g (70%) of quinoxalin-6-yl-acetic acid. 1H NMR (400 MHz, DMSO-d6) δ 12.6 (bs, 1H), 8.93 (dd, 2H, J=2.0, 6.0 Hz), 8.05 (d, 1H, 8.8 Hz), 7.99 (m, 1H), 7.79 (dd, 1H, J=2.0, 8.8 Hz), 3.89 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030305B2
Source datasetuspto-grants-2011_10
ORD IDord-186adc3f71b04d669682d969afba839b
Source noteuspto-grants-2011_10