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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Iodo-4-nitrobenzene | HCID 12495 | — |
| Reactant | N-(2,4-dimethoxybenzyl)prop-2-yn-1-amine | HCID 28419238 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N-(2,4-dimethoxybenzyl)-3-(4-nitrophenyl)prop-2-yn-1-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450320B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-1e12a24e45ac4167bdcd6a9daec620d5 |
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| Source note | uspto-grants-2013_05 |
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