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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049683Generated: November 1, 2026

2-Iodobenzoic acid → 2-[(4-Fluorophenyl)sulfanyl]benzoic acid

https://huagongshe.com/reaction/2049683

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Iodobenzoic acidHCID 6941—
ReactantPotassium CarbonateHCID 11430—
Reactant4-FluorothiophenolHCID 67789—
CatalystCopperHCID 23978—
SolventNitrobenzeneHCID 7416—
Product2-[(4-Fluorophenyl)sulfanyl]benzoic acidHCID 14418768—

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 147 g of iodobenzoic acid and 45.5 g of potassium carbonate in 57 ml of nitrobenzene is maintained with stirring at 160° C. for 40 minutes. Thereafter, 46.5 of additional potassium carbonate are added, followed by the addition of 73.1 g of 4-fluorothiophenol, another 46.5 g of potassium carbonate and 0.35 g of copper powder. The reaction mixture is stirred in a 160° C. bath for 45 minutes. The resulting solid is collected and then cooled to 0° C. before being mixed with 100 ml of water and 220 ml of 6 N hydrochloric acid. The aqueous mixture is then diluted to 1 liter total volume before being stirred with 450 ml of chloroform. The resulting residue white solid is collected and washed successively with chloroform and water. The solid is dissolved in hot acetone and the acetone solution is successively filtered and cooled to provide a white crystalline product. The product is recrystallized from acetone and then converted to a salt with potassium carbonate. The salt is dissolved in water and the aqueous solution is acidified with 1 N hydrochloric acid to provide 2-(4-fluorophenylthio)benzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04198420
Source datasetuspto-grants-1980_04
ORD IDord-157364e351c44b4981fb9fa4ac901c3e
Source noteuspto-grants-1980_04