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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484411Generated: October 30, 2026

Sodium methanethiolate → 5-Bromo-2-methylsulfanylmethyl-pyridine

https://huagongshe.com/reaction/1484411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactant5-bromo-2-(chloromethyl)pyridineHCID 11401501—
SolventDimethylformamideHCID 6228—
Product5-Bromo-2-methylsulfanylmethyl-pyridineHCID 11562235481%

Reaction Conditions

Temperature0 °C

Reaction Steps

To the stirred solution of 5-Bromo-2-chloromethyl-pyridine (3.5 gm, 16.99 mmol) in DMF (25 mL) at 0° C. is added Sodium thiomethoxide (1.31 gm, 18.68 mmol) resulting reaction mixture is stirred at 0° C. for 2 h. After completion quenched with water and extracted with ethyl acetate (3×100 mL). The Combined organic layer is washed with brine and organic layer dried over sodium sulphate, evaporate under reduced pressure. The crude is purified by column chromatography using silica 100-200 mesh using 10% EtOAc: Hexane as eluent to afford title compound (3 g) as brown colored liquid. 1NMR (400 MHz, DMSO) δ: 2.00 (s, 3H), 3.75 (s, 2H), 7.39 (d, J=8.32 Hz, 1H), 7.99-8.02 (dd, J1=2.44 Hz, J2=8.32 Hz, 1H), 8.60 (d, J=2.28 Hz, 1H). LC-MS (m/z): M+H=220.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422236B2
Source datasetuspto-grants-2016_08
ORD IDord-d131c5f4e7c041d196a4c2ed5a1a6949
Source noteuspto-grants-2016_08