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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512090Generated: October 30, 2026

Tributylvinyltin → HCID 86710146, compound

https://huagongshe.com/reaction/512090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 70818720HCID 70818720—
CatalystHCID 178418397HCID 178418397—
SolventChloroformHCID 6212—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86710146HCID 8671014627%

Reaction Steps

To a solution of 8 (85 mg, 0.864 mmol) in 1,4-dioxane (4 ml) were added lithium chloride (73.2 mg, 1.73 mmol), tetrakis(triphenylphosphine)palladium (99.8 mg, 10 mol %) and tributyl(vinyl)tin (0.327 ml, 1.12 mmol). The mixture was heated at reflux for 3 h then cooled and diluted with CHCl3. The mixture was washed with brine, dried over Na2SO4, filtered, and concentrated in under diminished pressure. The residue was purified by column chromatography on silica gel [AcOEt/MeOH (20:1)] to afford tert-butyl 3-hexadecyl-2,6-dimethyl-5-vinylpyridin-4-yl carbonate (10) (19 mg, 27%). 1H NMR (CDCl3) δ 0.02-0.03 (m, 3H), 1.20-1.27 (m, 28H), 1.46 (s, 9H), 2.45 (s, 3H), 2.48 (s, 3H), 2.54-2.56 (m, 2H), 5.55 (dd, 2H, J=17.6 Hz, 11.6 Hz) and 6.50 (dd, 1H, J=11.2 Hz, 11.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102626B2
Source datasetuspto-grants-2015_08
ORD IDord-06e32fc40429407e87078c202931a071
Source noteuspto-grants-2015_08