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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096037Generated: October 26, 2026

Hydrochloric Acid → 2-(2-Chloro-4-methoxy-phenyl)-1-quinoxalin-6-yl-ethanone

https://huagongshe.com/reaction/1096037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl 6-quinoxalinecarboxylateHCID 2781239—
Reactant2-(2-Chloro-4-methoxyphenyl)acetic acidHCID 4209132—
ReactantHCID 178418310HCID 178418310—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Chloro-4-methoxy-phenyl)-1-quinoxalin-6-yl-ethanoneHCID 66699230—

Reaction Steps

A 2M solution of tert-butylmagnesium chloride (CAS Reg. No. 677-22-5) in diethyl ether (5.9 ml) was added to 2-chloro-4-methoxyphenylacetic acid (1.173 g, CAS Reg. No. 91367-09-8) in THF (10 ml). The mixture was stirred at room temperature for 30 min. A solution of methyl 6-quinoxalinecarboxylate (1 g, CAS Reg. No. 23088-23-5) in THF (3 ml) was added and the resulting mixture was stirred overnight. Aqueous HCl (25%, 1.5 ml) and water (30 ml) were added and extracted with EtOAc. The combined organic layers were dried over Na2SO4 and then concentrated to an oil. The residue was purified by flash chromatography (SiO2, EtOAc/heptane 1:2) to give the title compound (480 mg) as a light brown solid. MS (m/e)=313.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138189B2
Source datasetuspto-grants-2012_03
ORD IDord-78c6a77ec643475aa983ef69075b0406
Source noteuspto-grants-2012_03