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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588782Generated: October 30, 2026

Tributylvinyltin → 4,5-Dichloro-2-vinylbenzenamine

https://huagongshe.com/reaction/588782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
Reactant4,5-Dichloro-2-iodoanilineHCID 10913187—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product4,5-Dichloro-2-vinylbenzenamineHCID 11760715476.7%

Reaction Steps

A mixture of 4,5-dichloro-2-iodobenzenamine (6 g, 20.8 mmol), tributyl(vinyl)stannane (6.6 g, 20.8 mmol), Pd(PPh3)4 (2.4 g, 2.1 mmol) in toluene (60 mL) was stirred at reflux under argon for 6 h. The mixture was allowed to cool to room temperature, quenched with aqueous KF solution and then extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel (petroleum ether/ethyl acetate=4:1) to afford the desired product (3.0 g, 76.7% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227978B2
Source datasetuspto-grants-2016_01
ORD IDord-6f33b6abcac94d31b5e4f9ea5fd9864e
Source noteuspto-grants-2016_01