Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384545Generated: October 31, 2026

Sodium hydride → HCID 22624918, compound

https://huagongshe.com/reaction/1384545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-(3-Bromopropoxy)tetrahydro-2H-pyranHCID 2777988—
ReactantHCID 178418642HCID 178418642—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 22624918HCID 2262491835.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium hydride (946 mg of a 50% suspension in mineral oil, 19.7 mmol) was added to a solution of 4-hydroxypyridine (1.88 g, 19.7 mmol) in DMF (50 ml) and the mixture stirred for 30 minutes. 2-(3-Bromopropoxy)tetrahydropyran (4.0 g, 17.9 mmol), (J. Chem. Soc. 1963, 3440), was added and the mixture heated at 100° C. for 3 hours. The reaction mixture was allowed to cool, diluted with water and extracted with ethyl acetate. The extract was washed with water, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with methylene chloride/methanol mixtures (100/0 increasing to 95/5) to give 1-[3-(tetrahydropyran-2-yloxy)propyl]-1,4-dihydro-4-pyridone (1.5 g, 35%). 1H NMR Spectrum: (DMSOd6) 1.35-1.75(m, 6H); 1.95(t, 2H); 3.35-3.5(m, 2H); 3.65-3.8(m, 2H); 4.12(t, 2H); 4.57(s, 1H); 6.95(s, 2H); 7.94(s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258951B1
Source datasetuspto-grants-2001_07
ORD IDord-8924b15788f24f5eb69b7b8f00b46c3c
Source noteuspto-grants-2001_07