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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| Reactant | 2-Fluoro-4-iodoaniline | HCID 185694 | — |
| Reactant | Tri(butyl)vinyltin | HCID 53438229 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Ethenyl-2-fluoroaniline | HCID 22025647 | 93% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642657B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-926e7f9b4a7b41be8c988492b8929abf |
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| Source note | uspto-grants-2014_02 |
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