HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410149Generated: October 29, 2026
Diethyl (ethoxymethylene)malonate → HCID 178469588, compound
https://huagongshe.com/reaction/2410149
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | P-Anisidine | HCID 7732 | — |
| Solvent | Diphenyl Ether | HCID 7583 | — |
| Product | HCID 178469588 | HCID 178469588 | 17% |
Reaction Steps
A mixture of 4-methoxyaniline (12.3 g, 100 mmol) and diethyl 2-(ethoxymethylene)malonate (21.6 g, 100 mmol) was stirred at 120° C. under nitrogen for 4 hrs. The solution was cooled to room temperature and Ph2O (100 mL) was added. The reaction mixture was refluxed at 260° C. under nitrogen for 8 hrs. The solution was cooled to room temperature and diluted with hexanes. The resultant precipitate was collected by filtration, washed with 25% ethyl acetate in hexanes, and dried under vacuum to give ethyl 4-hydroxy-6-methoxyquinoline-3-carboxylate as a pale-yellow solid (4.21 g, 17%). 1H NMR (400 MHz, DMSO-d6) δ 1.26 (t, J=7.0 Hz, 3H), 3.83 (s, 3H), 4.19 (q, J=7.0 Hz, 2H), 7.32 (dd, J=3.2, 9.6 Hz, 1H), 7.55 (d, J=3.2 Hz, 1H), 7.56 (d, J=9.6 Hz, 1H), 8.47 (s, 1H), 12.27 (s, 1H). MS 248 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815956B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-7a201f51c162447b8459ab36e98f1eca |
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| Source note | uspto-grants-2014_08 |
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