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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648262Generated: October 31, 2026

1,1'-Carbonyldiimidazole → Ethyl β-oxo-1H-imidazole-1-hexanoate

https://huagongshe.com/reaction/1648262

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantMonoethyl malonateHCID 70615—
ReactantImidazole-1-butyric acidHCID 3055390—
SolventTetrahydrofuranHCID 8028—
ProductEthyl β-oxo-1H-imidazole-1-hexanoateHCID 2209762744%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436247
Source datasetuspto-grants-1995_07
ORD IDord-4ac9d04d28c9430697401faf3f73566f
Source noteuspto-grants-1995_07