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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298938Generated: October 26, 2026

Triethylamine → 3-Amino-2-(4-chloro-phenylethynyl)-benzoic acid methyl ester

https://huagongshe.com/reaction/2298938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzene, 1-chloro-4-ethynyl-HCID 70118—
ReactantMethyl 2-iodo-3-nitrobenzoateHCID 264093—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTolueneHCID 1140—
Product3-Amino-2-(4-chloro-phenylethynyl)-benzoic acid methyl esterHCID 18340004—

Reaction Conditions

Temperature80 °C

Reaction Steps

2-iodo-3-nitro-benzoic acid methyl ester (0.79 g, 2.84 mmol), 1-chloro-4-ethynylbenzene (0.41 g, 2.99 mmol), palladium tetrakis(triphenylphosphine) (0.16 g, 0.14 mmol), copper (I) iodide (0.03 g, 0.14 mmol), and triethylamine (1.44 g, 14.19 mmol) were dissolved in 15 mL toluene. Argon was bubbled through the resulting solution for 15 min. The reaction was stirred under argon at 80° C. for 2 h and 20 min. The reaction mixture was then washed once with water, dried (MgSO4), and concentrated in vacuo. The orange oil was purified by flash chromatography eluting with 50 to 100% CHCl3/hexanes to yield 3-amino-2-(4-chloro-phenylethynyl)-benzoic acid methyl ester, 0.76 g (94%) as a yellow oil. 1H NMR (300 MHz, d6-DMSO) 3.84 (s,3H), 5.84 (br s, 2H), 6.97 (dd, J=8.1, 1.3 Hz, 1H), 7.05 (dd, J=7.5, 1.2 Hz, 1H), 7.17 (app t, J=7.5 Hz, 1H), 7.49 (d, J=8.7 Hz, 2H), 7.63 (d, J=8.7 Hz, 2H). MS (electrospray, MH+) 286.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495541B1
Source datasetuspto-grants-2002_12
ORD IDord-251d82ecfdb5474383d4ceee39789f9e
Source noteuspto-grants-2002_12