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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080922Generated: October 30, 2026

3-Ethynylbenzoyl chloride → HCID 86634500, compound

https://huagongshe.com/reaction/2080922

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Ethynylbenzoyl chlorideHCID 20038813—
ReactantSodium benzenethiolHCID 66586497—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86634500HCID 86634500—

Reaction Steps

Air in a 20 ml Schlenk tube was replaced by Ar gas and 1.02 g (7 mmol) of m-ethynylbenzoic acid and 5 g (42 mmol) of thionyl chloride were added to the tube and the mixture was stirred at 50° C. for 2 hours and then excess thionyl chloride was removed by distillation under reduced pressure to obtain m-ethynylbenzoyl chloride. To the m-ethynylbenzoyl chloride obtained was added 7 ml of THF and the resultant mixture was ice-cooled. Then, 971 mg (7.35 mmol) of sodium benzenethiol was added to the mixture and the resultant mixture was stirred at room temperature for 2 hours. After completion of the stirring, THF was removed by distillation under reduced pressure and 35 ml of water was added to the resultant residue. The mixture was extracted with 35 ml of ethyl acetate, the extract was dried over magnesium sulfate and the solvent was removed by distillation under reduced pressure using an evaporator. The resultant crude reaction product was purified by column chromatography (Hexane/AcOEt=20/1) using silica gel to obtain 0.51 g of S-phenyl 3-ethynyl-thiobenzoate which is a desired product as yellow solid. (Yield: 31%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932398B2
Source datasetuspto-grants-2011_04
ORD IDord-862c73b5cecd4d6eb640c817fff56de3
Source noteuspto-grants-2011_04