HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964583Generated: October 30, 2026
1,1'-Carbonyldiimidazole → Ethyl β-oxo-1H-imidazole-1-hexanoate
https://huagongshe.com/reaction/964583
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Monoethyl malonate | HCID 70615 | — |
| Reactant | Imidazole-1-butyric acid | HCID 3055390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl β-oxo-1H-imidazole-1-hexanoate | HCID 22097627 | 44% |
Reaction Steps
To a suspension of 4-(1-imidazolyl)butyric acid (0.5 g) in tetrahydrofuran (35 ml), 1,1'-carbonyldiimidazole (0.578 g) was added, followed by stirring at room temperature for 6 hours. After magnesium salt of malonic acid monoethyl ester [Mg(OCOCH2COOC2H5)2 ] (1.02 g) was added, the mixture was stirred at room temperature for 18 more hours. After the reaction mixture was concentrated under reduced pressure, the residue was dissolved in dichloromethane. The dichloromethane layer was washed with water and dried (MgSO4), after which the solvent was distilled off. The residual oily substance was subjected to silica gel column chromatography and eluted with chloroform-methanol (30:1, v/v) to yield 6-(1-imidazolyl)-3-oxohexanoic acid ethyl ester (0.32 g, 44%) as an oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05770602 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-3bbe189927fc4c66aa0e05d54c9d5a27 |
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| Source note | uspto-grants-1998_06 |
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