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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 266554Erstellt: 23. Oktober 2026

Carbon Dioxide → Benzoic acid, 2-(methylthio)-4-(trifluoromethyl)-

https://huagongshe.com/de/reaction/266554

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
EduktHydrochloric AcidHCID 313—
EduktBenzene, 1-bromo-2-(methylthio)-4-(trifluoromethyl)-HCID 11000144—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
ProduktBenzoic acid, 2-(methylthio)-4-(trifluoromethyl)-HCID 11085762—

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

n-Butyllithium (2.5M solution in hexane; 25 ml) was added under an inert atmosphere to a stirred solution 4-bromo-3-methylsulphenylbenzotrifluoride (16.4 g) in ether whilst maintaining the temperature below -70° C. The mixture was stirred at -70° C. for 2 hours and then poured onto solid carbon dioxide pellets. The mixture was stirred for 10 minutes and aqueous hydrochloric acid was added. The layers were separated and the aqueous layer was extracted with ether. The combined organic layers were washed with water, dried (anhydrous magnesium sulphate) and filtered. The filtrate was evaporated and the residue was triturated with cyclohexane and filtered to give 2-methylsulphenyl-4-trifluoromethylbenzoic acid (12.4 g) as a white solid, NMR [CDCl3 +DMSO-d6 ]: 2.45 (s,3H), 7.2(d, 1H), 7.3(s, 1H), 8.0 (d, 1H), 10.7-11.1 (bs, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05650533
Quelldatensatzuspto-grants-1997_07
ORD IDord-a6fbdd378e2747e8954f2dd49973b3d8
Quellennotizuspto-grants-1997_07