HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748369Generated: October 31, 2026
Diethyl (ethoxymethylene)malonate → HCID 135819170, compound
https://huagongshe.com/reaction/1748369
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | 3-Methoxyaniline | HCID 10824 | — |
| Reactant | Diethyl 2-(((3-methoxyphenyl)amino)methylene)malonate | HCID 3904966 | — |
| Product | HCID 135819170 | HCID 135819170 | 99% |
Reaction Steps
Diethyl 2-(((3-methoxyphenyl)amino)methylene)malonate. Diethyl ethoxymethylenemalonate (5.00 g, 40.6 mmol) and m-anisidine (8.13 mL, 40.6 mmol) were mixed and heated at 125° C. for 3 h. After cooling to ambient temperature, residual solvent was removed under reduced pressure and dried under high vacuum to afford the title compound as a yellow oil (11.81 g, 99%). 1H NMR (400 MHz, CDCl3) δ 11.57 (d, J=13.7 Hz, 1H), 9.11 (d, J=13.7 Hz, 1H), 7.90-7.83 (m, 1H), 7.31 (ddd, J=15.5, 8.2, 2.2 Hz, 2H), 7.25 (d, J=2.3 Hz, 1H), 4.90 (q, J=7.0 Hz, 2H), 4.84 (q, J=7.3 Hz, 2H), 4.42 (s, 3H), 1.98 (t, J=7.0 Hz, 3H), 1.92 (t, J=7.0 Hz, 3H). [M+H]=294.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150572B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-fae868f288a649f9be6ea80be265bf34 |
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| Source note | uspto-grants-2015_10 |
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