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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694036Generated: October 30, 2026

Dimethylformamide → 5-bromo-2-(phenylthio)pyridine

https://huagongshe.com/reaction/1694036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantThiophenolHCID 7969—
ReactantSodium hydrideHCID 24758—
Reactant2,5-DibromopyridineHCID 69353—
SolventWaterHCID 962—
Product5-bromo-2-(phenylthio)pyridineHCID 2218066799.7%

Reaction Steps

To an N,N-dimethylformamide (20 mL) solution of thiophenol (1.02 g, 9.28 mmol) was added sodium hydride (446 mg, 9.28 mmol, 50% in oil), which was stirred for 15 minutes at room temperature. 2,5-Dibromopyridine (2.00 g, 8.44 mmol) was then added to this reaction mixture and stirred for 35 minutes at room temperature, and then for a further 45 minutes at 55° C. Water was added to the reaction solution at room temperature, which was then extracted with ethyl acetate. The organic layer was separated, washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by NH silica gel column chromatography (heptane:ethyl acetate:=4:1) to obtain the title compound (2.24 g, quant.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158657B2
Source datasetuspto-grants-2012_04
ORD IDord-3aba66d6063f4222ac0a27cb70a82434
Source noteuspto-grants-2012_04