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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906233Generated: October 25, 2026

2-(4-Chlorophenethoxy)-3-methoxypyrazine → 3-(4-chlorophenethoxy)pyrazin-2(1H)-one

https://huagongshe.com/reaction/906233

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Chlorophenethoxy)-3-methoxypyrazineHCID 57540693—
ReactantHCID 178418395HCID 178418395—
SolventDimethylacetamideHCID 31374—
SolventSodium BicarbonateHCID 516892—
Product3-(4-chlorophenethoxy)pyrazin-2(1H)-oneHCID 5809240547.9%

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of benzo[d]thiazole-2-thiol (1.264 g, 7.56 mmol), 2-(4-chlorophenethoxy)-3-methoxypyrazine (1.00 g, 3.78 mmol) and NaHCO3 (1.587 g, 18.89 mmol) in DMA (10 mL) was stirred at 135° C. for 6 hours. After cooling to RT, the mixture was diluted with a solution of saturated NaHCO3 (55 ml) and was then extracted with EtOAc (60 ml). The EtOAc layer was dried over Na2SO4 and concentrated. The crude product was purified by silica gel chromatography employing a solvent gradient (hexane to 100% EtOAc) to elute 3-(4-chlorophenethoxy)pyrazin-2(1H)-one (477 mg, 1.808 mmol, 47.9% yield) as off-white solid. 1H NMR (400 MHz, chloroform-d) δ ppm 7.27-7.31 (2H, m), 7.19-7.25 (2H, m), 6.95 (1H, d, J=4.27 Hz), 6.89 (1H, d, J=4.52 Hz), 4.54 (2H, t, J=7.53 Hz), 3.14 (2H, t, J=7.40 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012984B2
Source datasetuspto-grants-2011_09
ORD IDord-d3bd87f326c5436c834c83ab687f4d84
Source noteuspto-grants-2011_09