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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75093Generated: October 30, 2026

Tributylvinyltin → HCID 86668301, compound

https://huagongshe.com/reaction/75093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantHCID 86668299HCID 86668299—
CatalystHCID 178418476HCID 178418476—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 86668301HCID 8666830176%

Reaction Steps

Methyl 4,6-dichloro-3-iodopicolinate (0.56 g, 1.7 mmol), vinyltributylstannane (580 μl, 0.63 g, 2.0 mmol) and bis(triphenylphosphine)palladium(II) chloride (0.12 g, 0.17 mmol) were combined in 1,2-dichloroethane (8 mL) and the mixture was sparged with a stream of nitrogen for 15 min. The reaction mixture was stirred at reflux for 21 h, cooled to room temperature, and diluted with ethyl acetate (15 mL). A solution of 20% KHF2 (10 ml) was added and the mixture was stirred for 45 minutes. The mixture was filtered through Celite. The organic phase was washed with water, washed with saturated sodium chloride, dried over sodium sulfate, and concentrated under vacuum. The crude product was purified by flash chromatography (SiO2, ethyl acetate/hexanes) to afford the title compound as a solid (0.30 g, 70%): 1H NMR (400 MHz, CDCl3) δ 7.50 (s, 1H), 6.82 (ddd, J=17.8, 11.5, 1.7 Hz, 1H), 5.66 (dd, J=11.4, 8.1 Hz, 1H), 5.55 (dt, J=17.7, 5.0 Hz, 1H), 3.92 (s, 3H); EIMS m/z 231.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835409B2
Source datasetuspto-grants-2014_09
ORD IDord-d2a30c93cda94a91a227a38b132d5e20
Source noteuspto-grants-2014_09