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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238936Generated: October 30, 2026

2,6-Di-tert-butyl-4-methylphenol → 4-Ethenyl-2-fluoroaniline

https://huagongshe.com/reaction/238936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
Reactant2-Fluoro-4-iodoanilineHCID 185694—
ReactantTri(butyl)vinyltinHCID 53438229—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product4-Ethenyl-2-fluoroanilineHCID 2202564793%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 2-fluoro-4-iodoaniline (2.37 g, 10 mmol) in toluene (50 mL) was treated with tetrakis(triphenylphosphine)palladium (0.578 g, 0.5 mmol), tributylvinyltin (3.5 mL, 12 mmol) and a catalytic amount of 2,6-di-tert-butyl-4-methylphenol. After being heated at 100° C. for 1 h, the reaction mixture was filtered through celite and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel using EtOAc:hexanes (1:5) as eluant to afford 2-Fluoro-4-vinylaniline (20-1, LJO-324, 1.275 g, 93%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642657B2
Source datasetuspto-grants-2014_02
ORD IDord-926e7f9b4a7b41be8c988492b8929abf
Source noteuspto-grants-2014_02