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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476697Generated: October 30, 2026

Sodium Carbonate → HCID 90412219, compound

https://huagongshe.com/reaction/1476697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantAmmonium HydroxideHCID 14923—
ReactantSodium AzideHCID 33557—
ReactantBenzene, 1-chloro-4-ethynyl-HCID 70118—
ReactantL-ProlineHCID 145742—
Reactant2-iodofuranHCID 11564629—
ReactantSodium AscorbateHCID 23667548—
Solvent(Methanesulfinyl)methane--water (1/1)HCID 23503278—
ProductHCID 90412219HCID 904122191.2%

Reaction Conditions

Temperature65 °C

Reaction Steps

A sealed tube was charged sequentially with 2-iodofuran (400 mg, 2.061 mmol), 1-chloro-4-ethynylbenzene (280 mg, 2.061 mmol), L-proline (47.4 mg, 0.412 mmol), Na2CO3 (44 mg, 0.412 mmol), sodium ascorbate (82 mg, 0.412 mmol), DMSO-H2O (9:1; 9 ml), NaN3 (160 mg, 2.47 mmol) and CuSO4.5H2O (514 mg, 2.061 mmol). The tube was sealed and stirred at 65° C. for 16 hours. The reaction mixture was then poured into a cold ammonium hydroxide solution, and the mixture was extracted with ethyl acetate (3×30 ml). The combined organic layers were washed with brine solution (30 ml), dried over sodium sulfate, and evaporated to yield the crude product, which was purified by column chromatography with 20% ethyl acetate/hexane to yield 4-(4-chlorophenyl)-1-(furan-2-yl)-1H-1,2,3-triazole (6 mg, 1.2%) as a pale yellow solid. The HPLC purity of the final product was 93.6%. LC-MS [M+1] 246 (C12H8ClN3O+H expected 246.04). The 1H-NMR spectra was in accordance with the chemical structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09402397B2
Source datasetuspto-grants-2016_08
ORD IDord-fe64b0bceb7c45e4881e0c5c24cee561
Source noteuspto-grants-2016_08