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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370343Generated: October 25, 2026

Carbon Dioxide → 4-(Pentafluoro-lambda6-sulfanyl)benzoic acid

https://huagongshe.com/reaction/370343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
Reactant1-Bromo-4-(pentafluoro-lambda6-sulfanyl)benzeneHCID 2779194—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product4-(Pentafluoro-lambda6-sulfanyl)benzoic acidHCID 277921035.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of n-butyllithium (9.4 ml of a 1.6 M solution in hexane) was added to a stirred solution of 4-bromophenylsulphur pentafluoride (3.87 g) in ether at -78° C. under an inert atmosphere. After maintaining at -78° C. for 1 hour, solid carbon dioxide (20 g) was added and the mixture allowed to warm to 5° C. during 1.5 hours. Hydrochloric acid (2 M) was added, the mixture stirred for 0.5 hour and the organic phase separated and itself extracted with sodium carbonate solution. The basic extract was washed (ether) and acidified (hydrochloric acid). The precipitated solid was extracted (ether), dried (magnesium sulphate) and evaporated. The residue was triturated (hexane) to give 4-pentafluorosulphanylbenzoic acid as a fawn solid (1.2 g), m.p.188-190° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140528
Source datasetuspto-grants-2000_10
ORD IDord-8592dd6c348f491c9eeb2151c7b550db
Source noteuspto-grants-2000_10