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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407243Generated: October 29, 2026

Tributylvinyltin → Methyl 4-amino-3-methoxy-6-vinylpicolinate

https://huagongshe.com/reaction/407243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantMethyl 4-amino-6-bromo-3-methoxypicolinateHCID 21696668—
CatalystHCID 178418476HCID 178418476—
Solvent1,2-DichloroethaneHCID 11—
ProductMethyl 4-amino-3-methoxy-6-vinylpicolinateHCID 8667541333%

Reaction Steps

Methyl 4-amino-6-bromo-3-methoxypicolinate (1 g, 3.83 mmol), tributyl(vinyl)stannane (1.822 g, 5.75 mmol) and bis(triphenylphosphine)palladium(II) chloride (0.403 g, 0.575 mmol) in DCE (12.77 ml) were stirred at 70° C. overnight. The mixture was adsorbed onto celite and purified by flash column chromatography (ISCO, SiO2 40 g, hexane/EtOAc 100:0 to 0:100 gradient) to afford methyl 4-amino-3-methoxy-6-vinylpicolinate (263 mg, 1.263 mmol, 33% yield) as a yellow oil. EIMS m/z 208; 1H NMR (400 MHz, CDCl3) δ 6.86 (s, 1H), 6.71 (dd, J=17.6, 10.9 Hz, 1H), 5.98 (dd, J=17.6, 1.0 Hz, 1H), 5.42 (dd, J=10.9, 1.0 Hz, 1H), 4.45 (s, 2H), 3.97 (s, 3H), 3.87 (s, 3H). 13C NMR (101 MHz, CDCl3) δ 165.94, 152.06, 148.02, 143.34, 141.60, 136.73, 118.02, 108.63, 61.49, 52.84.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754229B2
Source datasetuspto-grants-2014_06
ORD IDord-e3670bd5a3e6491a8aa72280debc2cc4
Source noteuspto-grants-2014_06