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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516539Generated: October 26, 2026

Tributylvinyltin → Methyl 4-amino-6-chloro-5-fluoro-3-vinylpicolinate

https://huagongshe.com/reaction/516539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantMethyl 4-amino-6-chloro-5-fluoro-3-iodopicolinateHCID 86668303—
CatalystHCID 178418476HCID 178418476—
Solvent1,1-DichloroethaneHCID 6365—
ProductMethyl 4-amino-6-chloro-5-fluoro-3-vinylpicolinateHCID 8666830965.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

Methyl 4-amino-6-chloro-5-fluoro-3-iodopicolinate (7.05 g, 21.33 mmol, prepared as described in Epp et al., WO 2013003740 A1) and vinyl tri-n-butyl tin (7.52 mL, 25.6 mmol) were suspended in dichloroethane (71.1 mL) and the mixture was degassed with Argon for 10 min. Bis(triphenylphosphine)palladium(II) chloride (1.497 g, 2.133 mmol) was then added and the reaction mixture was stirred at 70° C. overnight (clear orange solution). The reaction was monitored by GCMS. After 20 h, the reaction mixture was concentrated, adsorbed onto Celite™, and purified by column chromatography (SiO2, hexanes/ethyl acetate gradient) to afford the title compound as a light brown solid (3.23 g, 65.7%): mp 99-100° C.; 1H NMR (400 MHz, CDCl3) δ 6.87 (dd, J=18.1, 11.6 Hz, 1H), 5.72 (dd, J=11.5, 1.3 Hz, 1H), 5.52 (dd, J=18.2, 1.3 Hz, 1H), 4.79 (s, 2H), 3.91 (s, 3H); 19F NMR (376 MHz, CDCl3) δ −138.79 (s); EIMS m/z 230.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09113629B2
Source datasetuspto-grants-2015_08
ORD IDord-271528583ca749d18781991e0fb92480
Source noteuspto-grants-2015_08