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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712779Generated: October 29, 2026

Sodium methanethiolate → HCID 68756332, compound

https://huagongshe.com/reaction/712779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactant3-Bromo-5-(bromomethyl)pyridineHCID 14932948—
SolventEthanolHCID 702—
ProductHCID 68756332HCID 6875633291.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Bromo-5-bromomethyl-pyridine (7.5 g, 30 mmol) is dissolved in EtOH (200 mL). The solution is cooled down to 0° C. Sodium thiomethoxide (3.1 g, 45 mmol) is added slowly and the reaction mixture is stirred for 16 hrs. Then the solvent is removed, water and EtOAc are added. The aqueous layer is separated and extracted with EtOAc. Organic layers are combined and concentrated to give 6.0 g of the 3-bromo-5-methylsulfanylmethyl-pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181272B2
Source datasetuspto-grants-2015_11
ORD IDord-75ccd43aaee64bffbd201e16328c53a8
Source noteuspto-grants-2015_11