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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195285Generated: October 31, 2026

Sodium Hydroxide → 2-(1,3-Benzodioxol-5-yl)ethyl (pyridin-4-yl)methyl sulfide

https://huagongshe.com/reaction/1195285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-(Chloromethyl)pyridinium chlorideHCID 74570—
Reactant2-(1,3-Benzodioxol-5-yl)ethanethiolHCID 15819512—
SolventEthanolHCID 702—
Product2-(1,3-Benzodioxol-5-yl)ethyl (pyridin-4-yl)methyl sulfideHCID 1581951359.8%

Reaction Conditions

Temperature70 °C

Reaction Steps

3.30 g of 2-(1,3-benzodioxol-5-yl)ethanethiol was dissolved in 30 ml of ethanol. 1.65 g of sodium hydroxide and then 2.70 g of 4-picolyl chloride hydrochloride were added to the solution and the mixture was heated under reflux at 70° C. for 30 min. The solvent was distilled off and water was added to the residue. After extraction with ethyl acetate, 1N hydrochloric acid was added to the extract. The aqueous layer was acidified, taken up and washed with ethyl acetate. The pH of the aqueous layer was adjusted to 8 with potassium carbonate. After extraction with ethyl acetate, the extract was washed with a saturated aqueous common salt solution and dried over anhydrous magnesium sulfate. After filtration, the solvent was distilled off and the residue was purified according to silica gel column chromatography (ethyl acetate/hexane=1:4) to obtain 2.69 g of the intended compound in the form of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110956
Source datasetuspto-grants-1992_05
ORD IDord-5d3c633a1e88488fa36f60e3af9d51cc
Source noteuspto-grants-1992_05