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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096278Generated: November 2, 2026

1-Iodo-4-nitrobenzene → N-(2,4-dimethoxybenzyl)-3-(4-nitrophenyl)prop-2-yn-1-amine

https://huagongshe.com/reaction/2096278

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Iodo-4-nitrobenzeneHCID 12495—
ReactantN-(2,4-dimethoxybenzyl)prop-2-yn-1-amineHCID 28419238—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductN-(2,4-dimethoxybenzyl)-3-(4-nitrophenyl)prop-2-yn-1-amineHCID 67443629—

Reaction Steps

To a solution of EXAMPLE 23A (12.47 g, 60.83 mmol) in a mixture of N,N-dimethylformamide (150 mL) and triethylamine (150 mL) was added 1-iodo-4-nitrobenzene (18.18 g, 73 mmol), CuI (2.33 g, 12.2 mmol) and tetrakis(triphenylphosphine)palladium(0) (3.51 g, 3.04 mmol). The reaction mixture was stirred at room temperature overnight, and partitioned between ethyl acetate and brine. The organic phase was washed with brine, and concentrated. The crude material was purified by flash chromatography (20% ethyl acetate in hexane) to afford the title compound 1H NMR (400 MHz, dimethylsulfoxide-d6): δ 2.36 (br s, 1H), 3.59 (s, 2H), 3.72 (s, 2H), 3.74 (s, 3H), 3.77 (s, 3H), 6.48 (dd, J=6.0, 2.4 Hz, 1H), 6.53 (d, J=2.0 Hz, 1H), 7.20 (d, J=8.4 Hz, 1H), 7.67 (d, J=8.8 Hz, 2H), 8.22 (d, J=8.8 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450320B2
Source datasetuspto-grants-2013_05
ORD IDord-1e12a24e45ac4167bdcd6a9daec620d5
Source noteuspto-grants-2013_05