HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52137Generated: October 29, 2026
Acetic Anhydride → 2-Hydroxymethyl-3-methyl-4-(2-morpholinoethylthio)pyridine
https://huagongshe.com/reaction/52137
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2,3-dimethyl-4-(2-morpholinoethylthio)pyridine-N-oxide | HCID 19963100 | — |
| Product | 2-Hydroxymethyl-3-methyl-4-(2-morpholinoethylthio)pyridine | HCID 19963039 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616581 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-a98d48cb55634b7c9ce2564585732987 |
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| Source note | uspto-grants-1997_04 |
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