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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398839Generated: October 28, 2026

Tetrahydrofuran → HCID 18969211, compound

https://huagongshe.com/reaction/398839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 18969122HCID 18969122—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
ProductHCID 18969211HCID 1896921175.3%

Reaction Steps

Under ice-cooling, 2.9 g of 90% potassium tert-butoxide was added to 70 ml of tetrahydrofuran solution containing 6.4 g of N-(3-cyclohexylcarbonyl-2-pyridyl)-N-ethylacetamide, and the mixture was stirred at room temperature for 30 minutes. The reaction solution was mixed with water and extracted with ethyl acetate, and the resulting organic layer was dried over anhydrous magnesium sulfate. After removing magnesium sulfate by filtration, the filtrate was concentrated under reduced pressure and the resulting residue was purified by silica gel column chromatography (toluene-ethyl acetate) to give 4.5 g of 4-cyclohexyl-1-ethyl-1,8-naphthyridin-2(1H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05817670
Source datasetuspto-grants-1998_10
ORD IDord-90e1cfd6d5e74d6a9c8c8bb3ce9d5533
Source noteuspto-grants-1998_10