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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708468Generated: November 1, 2026

Tributylvinyltin → HCID 178435592, compound

https://huagongshe.com/reaction/1708468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantHCID 178441862HCID 178441862—
Catalyst2,6-Di-tert-butyl-4-methylphenolHCID 31404—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
ProductHCID 178435592HCID 17843559253.3%

Reaction Steps

A mixture of 12.28 g of 2-butyl-6-iodo-4(1H)-quinazolinone 0.866 g of tetrakis (triphenylphosphine)palladium, 0.015 g of 2,6-di-t-butyl-4-methylphenol in 75 ml of toluene and 20 ml of N,N-dimethylformamide is treated with 13.06 g of tri-n-butyl vinyltin followed by heating at reflux for 4 hours. The reaction mixture is cooled and concentrated in vacuo. The residue is diluted with hexanes and filtered. The filter cake is washed with hexanes and the remaining tacky solid dissolved in 100 ml of chloroform-methanol (8:2) and purified by chromato- graphy on silica gel with 1:3 ethyl acetate-hexanes to afford 4.55 g of the desired product as a yellow solid. CI MASS SPEC 229(MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05358951
Source datasetuspto-grants-1994_10
ORD IDord-592bbdf3ada247a6b7c4949e9fdbf0d9
Source noteuspto-grants-1994_10