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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354426Generated: November 1, 2026

Hydrochloric Acid → Ethyl 4-[5-(4-trifluoromethylphenyl)-2-thienyl]benzoate

https://huagongshe.com/reaction/1354426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 4-iodobenzoateHCID 142891—
Reactant2-[4-(Trifluoromethyl)phenyl]thiopheneHCID 12168056—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-[5-(4-trifluoromethylphenyl)-2-thienyl]benzoateHCID 2293454345%

Reaction Steps

To a solution (7 ml) of 2-(4-trifluoromethylphenyl) thiophene (1.71 g) in tetrahydrofuran was added dropwise n-butyl lithium (1.6 M solution in hexane, 5.00 ml) under an argon atmosphere at −78° C. This mixed solution was heated to room temperature, and a solution (14 ml) of zinc chloride (1.09 g) in tetrahydrofuran was added. This mixture was stirred for 1 hr., and ethyl 4-iodobenzoate (1.16 ml) and tetrakis(triphenylphosphine)palladium (0.202 g) were added. This mixture was stirred overnight under an argon atmosphere and poured into 0.5 M hydrochloric acid. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated. Ethanol (200 ml) was added to the residue, and the mixture was heated under reflux for 10 min. Insoluble materials were filtered off, and the filtrate was concentrated to give ethyl 4-[5-(4-trifluoromethylphenyl)-2-thienyl]benzoate (1.19 g, yield 45%) as a yellow crystalline powder. melting point: 203–204° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223791B2
Source datasetuspto-grants-2007_05
ORD IDord-dad12fbbd49c4f5bb795bd62e7296fcf
Source noteuspto-grants-2007_05