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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080918Generated: October 31, 2026

Phenol → HCID 23025175, compound

https://huagongshe.com/reaction/2080918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantPyridineHCID 1049—
Reactant3-Ethynylbenzoyl chlorideHCID 20038813—
SolventDichloromethaneHCID 6344—
ProductHCID 23025175HCID 23025175—

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 a solution having 692 mg (7.35 mmol) of phenol and 3.4 ml (42 mmol) of pyridine dissolved in 7 ml of dichloromethane under ice-cooling and then the resultant mixture was stirred at room temperature for one hour. After completion of the stirring, dichloromethane 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=10/1) using silica gel to obtain 0.55 q of phenyl 3-ethynylbenzoate which is a desired product as yellow solid. (Yield: 35%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932398B2
Source datasetuspto-grants-2011_04
ORD IDord-9837250d247241af9b546c267a8fd70b
Source noteuspto-grants-2011_04