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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21461Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/21461

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—

Reaktionsschritte

n-Butyllithium (2.5M in hexane, 25 ml) was added under an inert atmosphere to a stirred solution of 4-bromo-3-(methylsulphenyl)benzotrifluoride (16.4 g) in ether maintaining the temperature below -70° C. for 2 hours. The mixture was poured onto solid carbon dioxide pellets, stirred for 10 rains and aqueous hydrochloric acid added. The layers were separated and the aqueous layer was extracted with ether. The combined organic layers were washed with water, dried (MgSO4) 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(bs,1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05424276
Quelldatensatzuspto-grants-1995_06
ORD IDord-4b763ab9c11f46fdbe59706e9ea487f7
Quellennotizuspto-grants-1995_06