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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380208Generated: November 1, 2026

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

https://huagongshe.com/reaction/2380208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
ReactantBenzene, 1-bromo-2-(methylthio)-4-(trifluoromethyl)-HCID 11000144—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductBenzoic acid, 2-(methylthio)-4-(trifluoromethyl)-HCID 11085762—

Reaction Steps

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 mins 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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05366957
Source datasetuspto-grants-1994_11
ORD IDord-2a499f8b88ea4ea189c444fd84e51c09
Source noteuspto-grants-1994_11