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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2063193Erstellt: 27. Oktober 2026

Diisopropylamine → Benzene, 1-fluoro-2-(methylthio)-3-(trifluoromethyl)-

https://huagongshe.com/reaction/2063193

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
EduktDimethyl DisulfideHCID 12232—
Eduktalpha,alpha,alpha,3-TetrafluorotolueneHCID 67867—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBenzene, 1-fluoro-2-(methylthio)-3-(trifluoromethyl)-HCID 4145933—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Under an atmosphere of inert gas, 32.8 ml (1.6 M in hexane, 52.5 mmol) of n-butyllithium were added dropwise to a solution, cooled to 0° C., of 7.77 ml (55 mmol) of diisopropylamine in 100 ml of anhydrous tetrahydrofuran (THF), and after 10 minutes of stirring the solution was cooled to −78° C. 8.21 g (50 mmol) of 3-fluorobenzotrifluoride were added at this temperature, and the reaction mixture was stirred at this temperature for 1 h. 4.21 ml (55 mmol) of dimethyl disulfide were then added dropwise. Within about 3 h, the reaction mixture had warmed to room temperature (RT), and it was then once more cooled to 0° C. 10 ml of water were then added dropwise, and the reaction mixture was concentrated to about ¼ of its volume. The residue was taken up in water and dichloromethane, the phases were separated and the organic phase was washed successively with water, 10 percent strength hydrochloric acid, water, saturated aqueous NaHCO3 solution, water and saturated aqueous NaCl solution and dried over sodium sulfate and filtered. The solvent was removed and the residue was rectified under reduced pressure. This gave 8 g of 1-fluoro-2-methylthio-3-(trifluoromethyl)benzene of a boiling point of 68° C. at 6 mm Hg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08288319B2
Quelldatensatzuspto-grants-2012_10
ORD IDord-26e4d32909c345009c30937739b9f37e
Quellennotizuspto-grants-2012_10