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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351663Generated: October 24, 2026

Water → 1-(Phenylethynyl)-4-(phenylsulfonyl)benzene

https://huagongshe.com/en/reaction/1351663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantIodobenzeneHCID 11575—
Reactant4-PhenylsulfonylphenylethyneHCID 19939320—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
Product1-(Phenylethynyl)-4-(phenylsulfonyl)benzeneHCID 2109940328%

Reaction Steps

A mixture of 1-ethynyl-4-(phenylsulfonyl)benzene (100 mg, 0.4 mmol), iodobenzene (0.05 mL, 0.44 mmol) and triethylamine (1 mL) in toluene (1 mL) was degassed. Copper(I) iodide (3 mg, 0.004 mmol) and dichlorobis(triphenylphosphine)-palladium(II) (3 mg, 0.004 mmol) were added and the reaction stirred at room temperature overnight. The mixture was poured into water and extracted with ethyl acetate. The organic layer was dried and concentrated in vacuo. The residue was purified by preparative HPLC to give the title compound (35 mg, 28%). δH (500 MHz, d6 DMSO): 7.97 (4H, dd, J=2.6, 8.4 Hz), 7.77–7.69 (3H, m), 7.64–7.56 (4H, m), 7.43–7.41 (3H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217740B2
Source datasetuspto-grants-2007_05
ORD IDord-8973bec5db5f4dee8b621d09f2ec6299
Source noteuspto-grants-2007_05