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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108077Generated: October 25, 2026

Methyl 4-(3-mercaptophenyl)-3,4,5,6-tetrahydro-2H-pyran-4-carboxylate → Ethyl 4-[3-[4-(2-methylimidazol-1-yl)phenylthio]phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxylate

https://huagongshe.com/reaction/1108077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-(3-mercaptophenyl)-3,4,5,6-tetrahydro-2H-pyran-4-carboxylateHCID 11242202—
Reactant1-(4-iodophenyl)-2-methyl-1H-imidazoleHCID 11289090—
ReactantSodium t-butoxideHCID 23676156—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
ProductEthyl 4-[3-[4-(2-methylimidazol-1-yl)phenylthio]phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxylateHCID 1115443160.9%

Reaction Steps

A solution of methyl 4-(3-mercaptophenyl)-3,4,5,6-tetrahydro-2H-pyran-4-carboxylate (1.04 g, 3.5 mmol), 4-(2-methylimidazol-1-yl)phenyliodide (0.89 g, 3.5 mmol), sodium t-butoxide (673 mg, 7 mmol) and tetrakis(triphenylphosphine)palladium (162 mg, 0.14 mmol) in dry ethanol (20 ml) was heated to reflux with stirring overnight. Volatiles were remeved by evaporation and the residue was partitioned between ethyl acetate (100 ml) and water (100 ml). The aqueous layer was extracted with ethyl acetate (100 ml). The combined organic layers were washed with brine (100 ml), dried (magnesium sulfat) and concentrated to dryness to give 1.09 g of crude product as a brown liquid. Purification by column chromatography (silica-gel, 50 g; methanol in dichloromethane, increasing the ratio of methanol from 0% to 4%) afforded the titled compound (0.90 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06063928
Source datasetuspto-grants-2000_05
ORD IDord-c8111a64e6d54f2191828c98f2bea4d2
Source noteuspto-grants-2000_05