Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913154Generated: October 27, 2026

Pyridine, 2-(trimethylsilyl)- → Methyl [2,3'-bipyridine]-6'-carboxylate

https://huagongshe.com/reaction/1913154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine, 2-(trimethylsilyl)-HCID 139573—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantMethyl 5-bromopyridine-2-carboxylateHCID 7016458—
CatalystPalladium, di-mu-chlorobis(eta3-2-propenyl)di-HCID 61538—
CatalystHCID 178418778HCID 178418778—
SolventDimethylformamideHCID 6228—
ProductMethyl [2,3'-bipyridine]-6'-carboxylateHCID 5849456548%

Reaction Conditions

Temperature90 °C

Reaction Steps

This compound is synthesized as described by adaptation of the following reference: Tye et al., Tet. Lett., 2008, 49, 3939. To a stirred suspension of methyl-5-bromo-2-pyridine carboxylate (0.25 g, 1.16 mmol) and 2-(trimethylsilyl)pyridine (0.48 mL), 3.48 mmol) in anhydrous N,N-dimethyl formamide (7.5 mL) is added silver (I) oxide (0.27 g, 1.16 mmol), allyl palladium chloride dimer (21 mg, 5 mol %) and tetrabutyl ammonium fluoride (1M in THF, 0.116 mL). The reaction is heated at 90° C. for 18 h. The reaction mixture is filtered and washed with EtOAc. The filtrate is concentrated under reduced pressure. Purification by column chromatography (silica, eluent DCM, 0-2% MeOH) gives 0.12 g (48%) of methyl 2,3′-bipyridine-6′-carboxylate. m/z=215 [M++H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609696B2
Source datasetuspto-grants-2013_12
ORD IDord-b4ceba97887044c68ce83f751d27440b
Source noteuspto-grants-2013_12