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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080921Generated: October 28, 2026

Thionyl Chloride → 3-Ethynylbenzoyl chloride

https://huagongshe.com/reaction/2080921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-Ethynylbenzoic acidHCID 15897047—
Product3-Ethynylbenzoyl chlorideHCID 20038813—

Reaction Conditions

Temperature50 °C

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-165b685ea5744663a88f4d26cfa90ab4
Source noteuspto-grants-2011_04