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HRID 644458Erstellt: 24. Oktober 2026

5-Chloro-2-methoxyaniline → 5-Chloro-2-methoxy-beta-[3,5-bis(trifluoromethyl)phenyl]styrene

https://huagongshe.com/de/reaction/644458

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Chloro-2-methoxyanilineHCID 66763—
Edukt3,5-Bis(trifluoromethyl)styreneHCID 2773242—
EduktSodium NitriteHCID 23668193—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelTetrafluoroboric acidHCID 28118—
Produkt5-Chloro-2-methoxy-beta-[3,5-bis(trifluoromethyl)phenyl]styreneHCID 7654613834,7%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of sodium nitrite (57 mg, 0.8 mmol) in water (1 mL) was added to a solution of 2-amino-4-chloroanisole (131 mg, 0.8 mmol) in 48% hydrogen tetrafluoroborate (0.3 mL) under ice cooling and argon atmosphere. After the mixture was stirred at 0° C. for 1 hour, a solution of 3,5-bis(trifluoromethyl)styrene (100 mg, 0.4 mmol) in methanol (3 mL) was added and the mixture was stirred at 50° C. for 1 hour. After the reaction mixture was cooled to room temperature, the residue obtained by evaporation of the solvent under reduced pressure was diluted with ethyl acetate. After the solution was washed successively with 2N hydrochloric acid, water and brine, dried over anhydrous sodium sulfate, the residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give the title compound (52.8 mg, 33.3%) as a white powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07700655B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-84c38d26b4db498692231614c5f962f7
Quellennotizuspto-grants-2010_04