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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429710Generated: October 28, 2026

Iodine → HCID 178444342, compound

https://huagongshe.com/reaction/429710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium hydrideHCID 24758—
Reactant4-Ethoxy-2,3-difluorophenolHCID 14495763—
ReactantHCID 178444343HCID 178444343—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178444342HCID 17844434231.2%

Reaction Steps

To a suspension prepared by suspending 1.52 g (38.0 mmol) of 60% sodium hydride in 15 ml of THF was added dropwise solution of 5.29 g (17.3 mmol) of the 4-(trans-4-n-pentylcyclohexyl)-phenyldithiocarboxylic acid obtained by the first step, in 20 ml of THF under a condition cooled with ice in 15 min, and stirred as it was for 30 min. To this reaction solution was added dropwise solution of 2.50 g (14.4 mmol) of 2,3-difluoro-4-ethoxyphenol in 20 ml of THF in 15 min and stirred as it was for 30 min. To this reaction solution was added dropwise solution of 9.64 g (38.0 mmol) of iodine in 20 ml of THF in 15 min, stirred as it was for 1 hour, warmed up to room temperature, and then stirred at the same temperature overnight. This reaction solution was poured into 10% aqueous sodium thiosulfate solution and extracted with 100 ml of diethyl ether. The organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under a reduced pressure, and the residue was purified by silica gel column chromatography (eluent: heptane) and further recrystallized from heptane to obtain 2.0 g of 2,3-difluoro-4-ethoxyphenyl 4-(trans-4-n-pentylcyclohexyl)thiobenzoate (yield 31.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06319570B1
Source datasetuspto-grants-2001_11
ORD IDord-fbc2305469954ff2af47ce892fc1cfc4
Source noteuspto-grants-2001_11