HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378871Generated: October 25, 2026
Triethylamine → (E)-Diethyl 2-(4-amino-3-methyl-2-nitrobenzylidene)succinate
https://huagongshe.com/reaction/2378871
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl itaconate | HCID 75481 | — |
| Reactant | 4-Iodo-2-methyl-3-nitrobenzenamine | HCID 59731980 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (E)-Diethyl 2-(4-amino-3-methyl-2-nitrobenzylidene)succinate | HCID 59731889 | 42.8% |
Reaction Steps
To a solution of 4-iodo-2-methyl-3-nitrobenzenamine (59 mmol) in dimethylformamide (100 mL) was added diethyl itaconate (13.2 g, 71 mmol), tetrabutylammonium chloride (16.4 g, 59 mmol), triethylamine (236 mmol) and palladium acetate (675 mg, 3 mmol) under nitrogen. The reaction mixture was heated to 80° C. for 2 h. The crude reaction mixture was then filtered, diluted with ether (250 mL), washed with water (2×300 mL). The crude product was purified by flash chromatography using 20% ethyl acetate in hexane to give 8.5 g of the title compound. 1H NMR (500 MHz, CDCl3): in δ 7.58 (s, 1 H), 7.10 (d, J=8.5 Hz, 1H), 6.73 (d, J=8.5 Hz, 1 H), 4.24-4.15 (m, 4 H), 3.40 (s, 2 H), 2.06 (s, 3 H), 1.30-1.23 (m, 6 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07470680B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-c2cece78663545239c394b199bc96e7f |
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| Source note | uspto-grants-2008_12 |
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