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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175420Generated: November 2, 2026

tert-Butanol → (Z)-2-(2-tert-butoxyvinyl)-5-methylpyridine

https://huagongshe.com/reaction/2175420

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
Reactant2-Ethynyl-5-methylpyridineHCID 13400634—
ReactantPotassium tert-butoxideHCID 23665647—
Product(Z)-2-(2-tert-butoxyvinyl)-5-methylpyridineHCID 86729575—

Reaction Steps

To the solution of 2-ethynyl-5-methylpyridine (12-2) (1.38 g, 11.8 mmol) in tert-butyl alcohol (4.734 g, 63.9 mmol) was added potassium tert-butoxide (531 mg, 4.7 mmol) under nitrogen. The solution was heated to reflux for overnight. The solvent was removed under reduced pressure. The residue was purified by silca gel chromatography with the gradient eluent (PE/EA/NEt3=10/1/1%; 5/1/1%). The product (Z)-2-(2-tert-butoxyvinyl)-5-methylpyridine (12-3) was obtained as yellow oil (1.40 g, 62%) and by product was (E)-2-(2-tert-butoxyvinyl)-5-methylpyridine (0.3 g, 13%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062059B2
Source datasetuspto-grants-2015_06
ORD IDord-49e0f60196d24fdfae3616ed280245d7
Source noteuspto-grants-2015_06