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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422747Generated: November 2, 2026

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

https://huagongshe.com/reaction/1422747

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 numberUS08927542B2
Source datasetuspto-grants-2015_01
ORD IDord-05ac0c812ae64a7a988d2a6a7f5dbe18
Source noteuspto-grants-2015_01