HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910762Generated: November 1, 2026
Triethylamine → Methyl 3-(4-nitrophenyl)propiolate
https://huagongshe.com/reaction/1910762
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Iodo-4-nitrobenzene | HCID 12495 | — |
| Reactant | Methyl propiolate | HCID 13536 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3-(4-nitrophenyl)propiolate | HCID 251019 | 59% |
Reaction Steps
1-Iodo-4-nitrobenzene (2.5 g, 10 mmol) was added to a solution of triethylamine (2.0 g, 20 mmol) in THF (40 mL). PdCl2 (PPh3)2 (0.14 g, 0.20 mmol), cuprous iodide (0.076 g, 0.40 mmol) and methyl propiolate (3.4 g, 40 mmol) were added and the resulting mixture was heated to reflux overnight. The reaction mixture was cooled to r.t., the solvent evaporated, and the crude compound dissolved in dichloromethane. The organics were filtered to remove insoluble material and the filtrate was washed with water, brine solution and dried over sodium sulfate. The filtrate was concentrated and the residue purified over silica gel using 15% ethyl acetate in petroleum ether as eluent to afford (4-nitrophenyl)-propynoic acid methyl ester (1.20 g, 59%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604029B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-9347f1837b394c75a7048578f063a0cc |
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| Source note | uspto-grants-2013_12 |
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