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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188892Generated: November 1, 2026

Tributylvinyltin → 2,2-Dimethyl-N-(5-vinylpyridin-2-yl)-propionamide

https://huagongshe.com/reaction/2188892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantN-(5-bromopyridin-2-yl)-2,2-dimethylpropanamideHCID 15461537—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product2,2-Dimethyl-N-(5-vinylpyridin-2-yl)-propionamideHCID 2170207980.4%

Reaction Steps

Tributyl(vinyl)stannane (50 g, 0.16 mol), Pd(Ph3P)4 (3.3 g, 2.9 mmol) and a catalytic amount of 2,6-t-butyl-4-methylphenol was added to a solution of N-(5-bromopyridin-2-yl)pivalamide (36 g, 0.14 mol) in toluene. The reaction mixture was heated at reflux for 48 h. The solvent was evaporated in vacuo and the residue was purified by chromatography on silica gel (5% EtOAc in petroleum ether) to afford N-(5-vinylpyridin-2-yl)pivalamide (23 g, 80% yield). 1H NMR (CDCl3, 300 MHz) δ 8.24-8.20 (m, 2H), 8.02 (br s, 1H), 7.77 (dd, J=8.7 and 2.4, 1H), 6.65 (dd, J=17.7 and 10.8, 1H), 5.73 (d, J=17.7, 1H), 5.29 (d, J=10.8, 1H), 1.32 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324207B2
Source datasetuspto-grants-2012_12
ORD IDord-f9e44e3ebba44705bcd2b0e67cdfbf6f
Source noteuspto-grants-2012_12