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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1912874Erstellt: 26. Oktober 2026

4-Bromo-3-(trifluoromethyl)aniline → 3-Trifluoromethyl-4-vinylaniline

https://huagongshe.com/reaction/1912874

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Bromo-3-(trifluoromethyl)anilineHCID 67852—
EduktPotassium trifluorovinylborateHCID 86620274—
LösungsmittelWaterHCID 962—
LösungsmittelIsopropanolHCID 3776—
LösungsmittelTert-ButylamineHCID 6385—
Produkt3-Trifluoromethyl-4-vinylanilineHCID 2315517279,2%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

In 20 mL of isopropanol, 10 mL of water and 5 mL of t-butylamine, 4.0 g (16.7 mmol) of 4-bromo-3-(trifluoromethyl)aniline was dissolved, and 4.0 g (29.9 mmol) of potassium (trifluoro)vinylborate and 300 mg (0.37 mmol) of PdCl2(dppf)2•2(dichloromethane) complex were added thereto, and the mixture solution was stirred in an argon atmosphere at 80° C. for 20 hours. The reaction solution was concentrated and the residue was partitioned between water and ethyl acetate, and the organic layer was washed with a saturated sodium chloride solution and concentrated under reduced pressure. The product was purified by a silica gel column (n-hexane:ethyl acetate=6:1) to obtain 2.475 g (79%) of a target product as a pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08609656B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-744a22c9d51640a2a06e84a07a95c9aa
Quellennotizuspto-grants-2013_12