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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine, 2-(trimethylsilyl)- | HCID 139573 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | Methyl 5-bromopyridine-2-carboxylate | HCID 7016458 | — |
| Catalyst | Palladium, di-mu-chlorobis(eta3-2-propenyl)di- | HCID 61538 | — |
| Catalyst | HCID 178418778 | HCID 178418778 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl [2,3'-bipyridine]-6'-carboxylate | HCID 58494565 | 48% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08609696B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-b4ceba97887044c68ce83f751d27440b |
|---|
| Source note | uspto-grants-2013_12 |
|---|