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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 341736Erstellt: 26. Oktober 2026

Water → Benzene, 1-bromo-3-fluoro-4-(methylthio)-2-(trifluoromethyl)-

https://huagongshe.com/reaction/341736

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktDimethyl DisulfideHCID 12232—
EduktSodium NitriteHCID 23668193—
Edukt4-Bromo-2-fluoro-3-(trifluoromethyl)anilineHCID 53669714—
KatalysatorCopperHCID 23978—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelSulfuric AcidHCID 1118—
ProduktBenzene, 1-bromo-3-fluoro-4-(methylthio)-2-(trifluoromethyl)-HCID 53772445—

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

A solution of sodium nitrite (11.2 g) in concentrated sulphuric acid was added to a stirred cooled suspension of 4-bromo-2-fluoro-3-trifluoromethylaniline (40 g) in glacial acetic acid while maintaining the temperature below 5° C. The mixture was stirred at 5° C. for one and a half hours. The resultant mixture was added gradually to a mixture of dimethyl disulphide (20 ml) and copper power (0.224 g) in glacial acetic acid at 45° C. It was stirred and heated at 70° C. for 3 hours. It was cooled, poured into water, extracted with ether, washed with water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness and purified by column chromatography eluted with petroleum spirit (b.p. 60°-80° C.) to give 6-bromo-2-fluoro-3-(methylsulphenyl)benzotrifluoride (30.6 g) as an orange oil NMR (CDCl3) 2.45(s,3H), 7.25(t,1H), 7.5(d,1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05856274
Quelldatensatzuspto-grants-1999_01
ORD IDord-53ab50e7bcd246aa8df902be426b2b2b
Quellennotizuspto-grants-1999_01