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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207042Generated: November 2, 2026

Tributylvinyltin → 5-Bromo-7-methyl-6-vinylquinoline

https://huagongshe.com/reaction/2207042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantLithium ChlorideHCID 433294—
Reactant5-Bromo-7-methylquinolin-6-yl trifluoromethanesulfonateHCID 86691979—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product5-Bromo-7-methyl-6-vinylquinolineHCID 66630662—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-bromo-7-methylquinolin-6-yl trifluoromethanesulfonate (230 mg, 0.62 mmol), tributyl(vinyl)stannane (200 μL, 0.68 mmol), lithium chloride (78 mg, 1.86 mmol) and PdCl2(PPh3)2 (43 mg) in DMF (10 mL) was heated at 80° C. for 16 hours, and then the volatile component was removed in vacuo. The residue was dissolved in ethyl acetate (100 mL), washed with NaHCO3 solution, water and brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography (hexanes/EtOAc) to provide 5-bromo-7-methyl-6-vinylquinoline. LCMS-ESI+ (m/z): 248.2, 250.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376392B2
Source datasetuspto-grants-2016_06
ORD IDord-68a71b456ad74446b3468ff3348639c6
Source noteuspto-grants-2016_06