Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720044Generated: October 31, 2026

Acetic Anhydride → 2-Hydroxymethyl-3-methyl-4-(2-morpholinoethylthio)pyridine

https://huagongshe.com/reaction/1720044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2,3-dimethyl-4-(2-morpholinoethylthio)pyridine-N-oxideHCID 19963100—
Product2-Hydroxymethyl-3-methyl-4-(2-morpholinoethylthio)pyridineHCID 19963039—

Reaction Conditions

Temperature90 °C

Reaction Steps

2,3-Dimethyl-4-(2-morpholinoethylthio)pyridine-N-oxide (3.0 g) was dissolved in acetic anhydride (30 ml) and the mixture was stirred at 90° C. for 1.5 hours. The solvent was distilled away and water was added to the residue. The mixture was extracted with chloroform and dried over anhydrous magnesium sulfate, and the solvent was distilled away. The residual 2-acetoxymethyl-3-methyl-4-(2-morpholinoethylthio)pyridine (3.2 g) was dissolved in methanol (30 ml) and thereto was added sodium hydroxide (0.88 g) in water (10 ml) under ice-cooling. The mixture was stirred under ice-cooling for 1.5 hours and at room temperature for 2 hours. After the completion of the reaction, the methanol was distilled away and the residue was extracted with chloroform. The chloroform layer was dried over anhydrous magnesium sulfate and the solvent was distilled away to give 2.1 g of 2-hydroxymethyl-3-methyl-4-(2-morpholinoethylthio)pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05504082
Source datasetuspto-grants-1996_04
ORD IDord-d1de6928f1b94832aeb00582c029eb8f
Source noteuspto-grants-1996_04