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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279346Generated: October 30, 2026

2-Mercaptoethanol → 2-(7-Methoxy-quinoxalin-2-ylsulfanyl)-ethanol

https://huagongshe.com/reaction/2279346

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MercaptoethanolHCID 1567—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-7-methoxyquinoxalineHCID 12686415—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
Product2-(7-Methoxy-quinoxalin-2-ylsulfanyl)-ethanolHCID 6674625899%

Reaction Steps

2-Mercaptoethanol (2.5 g, 32.06 mmol, 1.2 eq) is added at room temperature to a stirred solution of 2-chloro-7-methoxy-quinoxaline (5.2 g, 26.72 mmol, 1.0 eq) in N,N-dimethylformamide (160 mL), followed by potassium carbonate (7.4 g, 53.44 mol, 2.0 eq). After 15 hours stirring at room temperature, solvent is evaporated and the residue is extracted with ethyl acetate (3×150 mL) and water (100 mL). The combined organic layers are dried over sodium sulfate, filtered and concentrated to give a crude product that is purified by column chromatography (silica gel, eluent: ethyl acetate:hexane, 1:2, v/v) to afford 2-(7-methoxy-quinoxalin-2-ylsulfanyl)-ethanol as a pale yellow solid (6.22 g, 99% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133219B2
Source datasetuspto-grants-2015_09
ORD IDord-fa0be831a9fb4897a00d2cbf525611ba
Source noteuspto-grants-2015_09