Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623606Generated: November 1, 2026

Sodium Methoxide → HCID 24988169, compound

https://huagongshe.com/reaction/1623606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 68468291HCID 68468291—
ReactantHCID 178527775HCID 178527775—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 24988169HCID 2498816938.7%

Reaction Steps

To a liquid prepared by dissolving with stirring 8.7 g (0.058 mol, 0.95 eq.) of 2-mercaptobenzimidazole and 68.2 g (0.354 mol, 5.8 eq.) of a 28% sodium methoxide solution in 400 mL of methanol, a liquid prepared by dissolving the whole amount of 4-heptyloxy-2-chloromethyl-3-methylpyridine in 210 mL of methanol was added at 28° C. Subsequently, the mixture was heated to reflux for one hour and cooled, and then methanol was solid dried under reduced pressure. A yellow brown oily residue resulting therefrom was dissolved in 250 mL of ethyl acetate, and then the organic layer was washed with 100 mL of water. The organic layer was dried over anhydrous magnesium sulfate, and then concentrated to dryness. The resulting residue was purified by silica gel column chromatography, and then was concentrated to dryness, to obtain 17.8 g of an orange-colored oily matter. The orange-colored oily matter was recrystallized from ethyl acetate (7 vol.), to obtain 8.7 g of colorless crystals (HPLC: 99.0 Area %, yield 38.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778975B2
Source datasetuspto-grants-2014_07
ORD IDord-6437fe03dcba4d7e9b7ae6255bddd2d4
Source noteuspto-grants-2014_07