HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289922Generated: October 31, 2026
Diethyl (ethoxymethylene)malonate → HCID 178469614, compound
https://huagongshe.com/reaction/2289922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | 3-Iodoaniline | HCID 12271 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178469614 | HCID 178469614 | — |
Reaction Steps
3-Iodoaniline (8.50 mL) and diethyl ethoxymethylenemalonate (14.30 mL) are heated at 130° C. for 1 hour. The reaction is cooled to room temperature and 70 mL diphenyl ether is added. The solution is heated at 250° C. for 1.5 hours with removal of ethanol by a Dean-Stark trap. The reaction is cooled to room temperature and the resulting solid filtered, washed with hexanes, and dried. The solid is triturated in ethyl acetate to give 12.82 g of ethyl 4-hydroxy-7-iodoquinoline-3-carboxylate. A mixture of this ester (0.35 g) and 4-chlorobenzylamine (3.0 mL) are heated at 180° C. for 1 hour. The reaction is cooled to 70° C. and poured into 50 mL diethyl ether. A tan solid which crystallizes slowly out of diethyl ether is obtained. The solid is recrystallized from ethyl acetate/hexanes to give the desired product (0.22 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06093732 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-436bd966023e4fd3b7deb97a1c033e87 |
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| Source note | uspto-grants-2000_07 |
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