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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354417Generated: November 2, 2026

Hydrochloric Acid → HCID 22934531, compound

https://huagongshe.com/reaction/1354417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 4-iodobenzoateHCID 142891—
ReactantHCID 22934551HCID 22934551—
ReactantHCID 178418306HCID 178418306—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22934531HCID 2293453131%

Reaction Steps

To a solution (5 ml) of 1-methyl-2-(4-trifluoromethylphenyl)pyrrole (1.13 g) in tetrahydrofuran was added dropwise t-butyl lithium (1.7 M solution in pentane, 3.00 ml) under an argon atmosphere at −78° C. This mixed solution was heated to room temperature, and a solution (10 ml) of zinc chloride (0.756 g) in tetrahydrofuran was added. This mixture was stirred for 1 hr., and ethyl 4-iodobenzoate (0.381 ml) and tetrakis (triphenylphosphine)palladium (0.144 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, and the organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=7:1, volume ratio) and recrystallized from hexane-ethyl acetate to give ethyl 4-[1-methyl-5-(4-trifluoromethylphenyl)-2-pyrrolyl]benzoate (0.573 g, yield 31%) as colorless needle crystals. melting point: 150–151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223791B2
Source datasetuspto-grants-2007_05
ORD IDord-1e17f899ded54ae4a012efc0d5a145ce
Source noteuspto-grants-2007_05