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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489557Generated: October 25, 2026

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

https://huagongshe.com/reaction/489557

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) δ 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 numberUS06977298B2
Source datasetuspto-grants-2005_12
ORD IDord-d6494735342649c79e2341aaf772efbf
Source noteuspto-grants-2005_12