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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051142Generated: November 4, 2026

Tributylvinyltin → HCID 86710144, compound

https://huagongshe.com/reaction/1051142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 70818934HCID 70818934—
CatalystHCID 178418397HCID 178418397—
SolventChloroformHCID 6212—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86710144HCID 8671014464%

Reaction Steps

To a solution of 7 (60 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-heptyl-2,6-dimethyl-5-vinylpyridin-4-yl carbonate (9) (30 mg, 64%). 1H NMR (CDCl3) δ 0.85-0.88 (m, 3H), 1.27-1.32 (m, 10H), 1.47 (s, 9H), 2.40 (s, 3H), 2.43 (s, 3H), 2.47-2.50 (m, 2H), 5.50 (dd, 2H, J=18 Hz, 11.2 Hz) and 6.45 (dd, 1H, J=11.6 Hz, 11.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388163B2
Source datasetuspto-grants-2016_07
ORD IDord-81d66b0371d449daa5255ec53eb24b77
Source noteuspto-grants-2016_07