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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354423Generated: November 1, 2026

Hydrochloric Acid → HCID 21105765, compound

https://huagongshe.com/reaction/1354423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-(4-Trifluoromethylphenyl)furanHCID 10656151—
ReactantHCID 22934559HCID 22934559—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21105765HCID 2110576543%

Reaction Steps

To a solution (25 ml) of 2-(4-trifluoromethylphenyl)furan (3.18 g) in tetrahydrofuran was added dropwise n-butyl lithium (1.6 M solution in hexane, 10.0 ml) under an argon atmosphere at −78° C. This mixed solution was heated to room temperature, and a solution (30 ml) of zinc chloride (2.25 g) in tetrahydrofuran was added. This mixture was stirred for 1 hr., and benzyl 2-benzyloxy-5-iodobenzoate (6.66 g) and tetrakis (triphenylphosphine)palladium (0.433 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. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1, volume ratio) and recrystallized from hexane-ethyl acetate to give benzyl 2-benzyloxy-5-[5-(4-trifluoromethylphenyl)-2-furyl]benzoate (3.41 g, yield 43%) as pale-yellow needle crystals. melting point: 97–98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223791B2
Source datasetuspto-grants-2007_05
ORD IDord-c619513b6b8f463e8595bf5d5386c4a3
Source noteuspto-grants-2007_05