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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298441Generated: October 29, 2026

Hydrochloric Acid → Ethyl 4-[2-(2,5-dimethylpyrrole-1-yl)ethoxy]acetoacetate

https://huagongshe.com/reaction/2298441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 4-chloroacetoacetateHCID 69484—
Reactant1-(2-Hydroxyethyl)-2,5-dimethylpyrroleHCID 95963—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-[2-(2,5-dimethylpyrrole-1-yl)ethoxy]acetoacetateHCID 1136915490%

Reaction Steps

32 g of sodiumhydride (60% oil dispersion) was added to 500 ml of tetrahydrofuran, and 56 g (0.4 mol) of 2-(2,5-dimethylpyrrole-1-yl)ethanol obtained in Preparation Example 1 was added thereto, followed by stirring at room temperature for 1 hour. The reaction mixture was cooled to 0° C., and a solution obtained by dissolving 65.84 g (0.4 mol) of ethyl 4-chloroacetoacetate in 200 ml of tetrahydrofuran was added thereto dropwise over 2 hours. The mixture was stirred at room temperature for 16 hours and then adjusted to pH 6 to 7 with 3N hydrochloric acid. A sufficient amount of water was added to dissolve solid precipitates formed, and the reaction mixture was extracted two times with 600 ml and 100 ml of ethyl acetate, respectively. Combined ethyl acetate extract was dried over anhydrous magnesium sulfate, treated with decolorizing carbon, and then, the solvent was distilled off under a reduced pressure, to obtain 96.2 g of the titled compound as a pale yellow oil (yield: 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492523B2
Source datasetuspto-grants-2002_12
ORD IDord-a64c17012b894b379b078732d70d8f60
Source noteuspto-grants-2002_12