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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22887Generated: October 30, 2026

Methanol → 5-(Methylthio)-2-nitropyridine

https://huagongshe.com/reaction/22887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant5-Chloro-2-nitropyridineHCID 259806—
ReactantSodium methanethiolateHCID 4378561—
SolventWaterHCID 962—
Product5-(Methylthio)-2-nitropyridineHCID 2203618245.3%

Reaction Steps

A methanol (40 mml) solution of 5-chloro-2-nitropyridine (2.0 g, 12.6 mmol) was added dropwise to a methanol (20 ml) solution of sodium thiomethoxide (1.02 g, 13.9 mmol) while being cooled with ice, and after the mixture was stirred for 13 hours while raising its temperature to the room temperature, water added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with water and then with a saturated aqueous solution of sodium chloride, and dried over magnesium sulfate. Thereafter, the solvent was distilled off, and the resulting crude product was recrystalized with ethyl acetate-hexane to obtain 972 mg (yield 45%) of 5-methylthio-2-nitropyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849647B1
Source datasetuspto-grants-2005_02
ORD IDord-842529a3c59a462ca41cefde3aef85fc
Source noteuspto-grants-2005_02