HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535463Generated: October 30, 2026
Diethyl (ethoxymethylene)malonate → HCID 66653275, compound
https://huagongshe.com/reaction/535463
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Pentane | HCID 8003 | — |
| Reactant | HCID 66653091 | HCID 66653091 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diphenyl Ether | HCID 7583 | — |
| Product | HCID 66653275 | HCID 66653275 | — |
Reaction Steps
0.36 ml of diethyl ethoxymethylene malonate is added, under an inert atmosphere at ambient temperature, to 0.4 g (1.43 mmol) of (4-aminophenyl)(1-methoxy-2-methylindolizin-3-yl)methanone in 6 ml of toluene. The reaction medium is heated at 110° C. for 1 h 45 and then concentrated under reduced pressure. The residue obtained is dissolved in 8.2 ml of diphenyl ether and then heated at 230° C. for 1 h 20. After the addition of diisopropyl ether and pentane at ambient temperature, the precipitate formed is filtered off and rinsed with pentane. The residue obtained is purified by silica gel column chromatography, elution being carried out with a dichloromethane/methanol (90/10) mixture. 142 mg of a yellow powder are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859544B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-a48e68fef1d84b809624b224352e9f8f |
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| Source note | uspto-grants-2014_10 |
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