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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75091Generated: October 30, 2026

Tributylvinyltin → Methyl 4-amino-5,6-dichloro-3-vinylpicolinate

https://huagongshe.com/reaction/75091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantHCID 86668298HCID 86668298—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-amino-5,6-dichloro-3-vinylpicolinateHCID 57412109184.6%

Reaction Steps

Methyl 4-amino-5,6-dichloro-3-iodopicolinate (0.5 g, 1.4 mmol), vinyltributylstannane (530 μl, 0.57 mmol, 1.8 mmol), and bis(triphenylphosphine)palladium(II) chloride (0.10 g, 0.1 mmol) were combined in nitrogen-deaerated 1,2-dichloroethane (10 mL). The reaction mixture was heated at reflux for 8 hours. The cooled reaction mixture was diluted with ethyl acetate (30 mL) and stirred with 15% KHF2 solution (10 mL) for 30 minutes. The phases were separated and the aqueous phase was extracted with ethyl acetate. The combined organic phases were washed with saturated sodium chloride, dried over sodium sulfate, and concentrated under vacuum. The crude product was purified by flash chromatography (SiO2, ethyl acetate/hexane) to afford the title compound as a tan solid (0.26 g, 73%): mp 96-97° C.; 1H NMR (400 MHz, CDCl3) δ 6.85 (dd, J=18.1, 11.5 Hz, 1H), 5.72 (dd, J=11.5, 1.3 Hz, 1H), 5.53 (dd, J=18.1, 1.3 Hz, 1H), 5.19 (s, 2H), 3.91 (s, 3H); EIMS m/z 246 ([M−H)−].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835409B2
Source datasetuspto-grants-2014_09
ORD IDord-091419462fdf4cafad94a2237323b3be
Source noteuspto-grants-2014_09