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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384633Generated: October 31, 2026

Sodium hydride → HCID 22625067, compound

https://huagongshe.com/reaction/1384633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-(3-Bromopropoxy)tetrahydro-2H-pyranHCID 2777988—
ReactantHCID 178480602HCID 178480602—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 22625067HCID 2262506755%

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium hydride (0.95 g of a 50% suspension in mineral oil, 20 mmol) was added to a solution of 2-mercapto-1-methylimidazole (2.26 g, 19 mmol) in DMF (100 ml) and the mixture stirred for 30 minutes. 2-(3-Bromopropoxy)tetrahydropyran (5.0 g, 22.5 mmol), (J. Chem. Soc. 1963, 3440), was added and the mixture heated at 100° C. for 3 hours and then stirred at ambient temperature for 18 hours. The reaction mixture was diluted with water and extracted with ethyl acetate. The combined extracts were 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 97/3) to give 1-methyl-2-(3-(2-tetrahydropyranyloxy)propylthio)imidazole (2.5 g, 55%). 1H NMR Spectrum: (DMSOd6) 1.38-1.72(m, 6H); 1.80(m, 2H); 3.0(t, 2H); 3.36-343(m, 2H); 3.58(s, 3H); 3.62-3.78(m, 2H); 4.50(s, 1H); 6.90(s, 1H); 7.21(s, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258951B1
Source datasetuspto-grants-2001_07
ORD IDord-b0ec1a8b36264c2ebb6fb8810472dc7a
Source noteuspto-grants-2001_07