HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070596Generated: October 29, 2026
Diethyl (ethoxymethylene)malonate → HCID 22397174, compound
https://huagongshe.com/reaction/1070596
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | 2-Pyridinamine, 5-iodo- | HCID 88579 | — |
| Product | HCID 22397174 | HCID 22397174 | 32% |
Reaction Steps
In a 3-necked round-bottom connected to a Dean-Stark trap, a solution of 2-amino-5-iodopyridine (Preparation 1, 500 mg) and diethyl ethoxymethylenemalonate (0.92 mL) is heated at 130° C. for 2 h. The reaction is cooled to room temperature. Diphenyl ether (5 mL) is added and the reaction is heated at 250° C. for 1 h. Upon cooling the mixture to room temperature, a solid precipitates and is filtered and washed with hexanes. The crude solid is adsorbed onto silica and chromatographed eluting with CH2Cl2 (2 L). Product-containing fractions are combined and concentrated to afford a solid. The crude product is recrystallized from CH2Cl2/hexanes to yield 251 mg (32%) of the title compound as a yellow solid. Physical characteristics: m.p. 166-168° C.; 1H NMR (300 MHz, DMSO-d6) δ9.24, 8.85, 8.38, 7.62, 4.27, 1.30; IR (drift) 1747, 1611, 1558, 1506, 1473, 1355, 1345, 1291, 1266, 1258, 1152, 1140, 1118, 840, 796 cm−1; MS (ESI+) m/z 345; Anal. found: C, 38.37; H, 2.48; N, 8.11.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06903097B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-daad8b1eab6b4f509708924666cc32f2 |
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| Source note | uspto-grants-2005_06 |
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