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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470640Generated: October 25, 2026

4-Ethynyl-1,1'-biphenyl → 2-Amino-3-biphenyl-4-ylethynyl-benzoic acid methyl ester

https://huagongshe.com/reaction/1470640

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Ethynyl-1,1'-biphenylHCID 34464—
ReactantMethyl 2-amino-3-iodobenzoateHCID 21258150—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-3-biphenyl-4-ylethynyl-benzoic acid methyl esterHCID 6670634276.4%

Reaction Steps

To a solution of 2-amino-3-iodo-benzoic acid methyl ester (500 mg, 1.8 mmol), 4-ethynyl-biphenyl (416 mg, 2.3 mmol) in THF (20 mL), CuI (17 mg, 0.09 mmol), bis-(triphenylphosphine)-palladium (II)-chloride (64 mg, 0.09 mmol) and TEA (0.75 mL, 5.4 mmol) were added. This mixture was stirred at room temperature for 12 h. The progress of the reaction was monitored by TLC. After completion, the reaction mass was filtered through celite, and the collected filtrate was diluted with ethyl acetate (30 mL), washed with water (2×20 mL) and the combined organic layer was separated and dried over sodium sulphate and concentrated under reduced pressure to obtain brown mass which was purified by column chromatography using 5% ethyl acetate in hexane as an eluent to obtain 450 mg of 2-amino-3-biphenyl-4-ylethynyl-benzoic acid methyl ester as a pale yellow coloured solid (76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006454B2
Source datasetuspto-grants-2015_04
ORD IDord-ec4b4a98675e4a7e8de6f7f7588ea4e5
Source noteuspto-grants-2015_04