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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422259Generated: November 3, 2026

Hydrochloric Acid → HCID 18706394, compound

https://huagongshe.com/reaction/1422259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPropargyl alcoholHCID 7859—
ReactantTriethylamineHCID 8471—
ReactantHCID 18706701HCID 18706701—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 18706394HCID 1870639410.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

12.9 g (36.8 mmol) of 7-chloro-2,3-dimethoxy-5-iodo-quinoxaline, 7.6 ml (128.4 mmol) of propargyl alcohol, 2.1 g (3 mmol) of bis(triphenylphosphine)-palladium dichloride, 6.6 ml (47.4 mmol) of triethylamine and 0.34 g (1.8 mmol) of cuprous iodide are placed in 125 ml of dimethylformamide and heated to a bath temperature of 70° C. The reaction mixture is then stirred for 3.5 hours at that temperature and then cooled to room temperature. Ethyl acetate is added to the reaction mixture and extraction is carried out with water, 1N hydrochloric acid and brine. The aqueous phases are washed with ethyl acetate. The organic phases are combined, dried over sodium sulfate, filtered with suction and concentrated. Chromatography of the crude product on silica gel with hexane/ethyl acetate (3:1) yields 1.1 g of 3-(7-chloro-2,3-dimethoxy-quinoxalin-5-yl)-prop-2-yn-1-ol in the form of brown crystals having a melting point of 137-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080743
Source datasetuspto-grants-2000_06
ORD IDord-00622cf26dbb45478c3038fdde33a6f3
Source noteuspto-grants-2000_06