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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924855Generated: November 1, 2026

Sodium methanethiolate → 2-Chloro-3-methoxy-5-methylthiomethylpyridine

https://huagongshe.com/reaction/1924855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactant2-Chloro-5-(chloromethyl)-3-methoxypyridineHCID 59297073—
SolventEthanolHCID 702—
Product2-Chloro-3-methoxy-5-methylthiomethylpyridineHCID 59297084—

Reaction Steps

To a suspension of sodium thiomethoxide (0.24 g, 3.5 mmol) in ethanol (10 mL) at 25° C. was added solution of 2-chloro-5-chloromethyl-3-methoxypyridine (0.55 mg, 2.9 mmol) in EtOH (4 mL). The solution was stirred overnight, after which the reaction was concentrated under vacuum. The crude reaction mixture was partitioned between H2O and Et2O and the layers separated. The aqueous phase was further extracted with Et2O (3×) and the combined organic phases dried over MgSO4 and concentrated to furnish 2-chloro-3-methoxy-5-methylthiomethylpyridine as a yellow oil (0.42 g, 71% over two steps). GC-MS: Exact mass calcd for C8H10ClNOS [M]+, 203. Found 203.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178565B2
Source datasetuspto-grants-2012_05
ORD IDord-b24bfacfbd014f6d89a1289f5bd138b3
Source noteuspto-grants-2012_05