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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080916Generated: October 31, 2026

Methanol → Ethyl 3-ethynylbenzoate

https://huagongshe.com/reaction/2080916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPyridineHCID 1049—
Reactant3-Ethynylbenzoyl chlorideHCID 20038813—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductEthyl 3-ethynylbenzoateHCID 15540684—

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 298 μl (7.35 mmol) of methanol 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 and extracted with 35 ml of diethyl ether. The ether layer was dried over magnesium sulfate and the solvent was removed by distillation under reduced pressure using an evaporator. The resultant crude reaction product was dissolved in 15 ml of hexane at 70° C., insoluble matter was removed by filtration and the filtrate was cooled to obtain 0.74 g of ethyl 3-ethynylbenzoate which is a desired product as yellow solid. (Yield: 66E)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932398B2
Source datasetuspto-grants-2011_04
ORD IDord-fd6baa8fe88c49c2b33b5a9bb0dc5525
Source noteuspto-grants-2011_04