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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679242Generated: November 2, 2026

Water → 1-(Ethoxycarbonylmethyl)-2-piperidone

https://huagongshe.com/reaction/1679242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl bromoacetateHCID 7748—
Reactant2-PiperidoneHCID 12665—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1-(Ethoxycarbonylmethyl)-2-piperidoneHCID 10750014—

Reaction Steps

9.9 parts of δ-valerolactam (purchased from Aldrich Chemical Co., Milwaukee, Wisc. 53233) were dissolved in 100 part of dimethylformamide. To this solution was added 4.8 parts of a 50% dispersion of sodium hydride in mineral oil (purchased from Callgary Chemical Company, Callgary, Pa.). The reaction mixture was stirred for a period of 30 minutes. To the above reaction mixture 16.7 parts of ethylbromoacetate was added dropwise keeping the temperature less than 25° C during the addition. After the addition was completed, the reaction was stirred at room temperature for an additional 30 minutes. The reaction mass was poured into 200 parts of water. The product was isolated by extraction from the aqueous solution with three successive 200-part portions of methylene chloride. The combined organic extracts of the product were dried with anhydrous sodium sulfate. The solution of the product was filtered and the solvent was removed by evaporation at a reduced pressure of 50-300 mm on a rotary evaporator. The crude product obtained was further purified by vacuum distillation at 115° -120° C at 1.5 mm; 8.2 parts of product were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04080192
Source datasetuspto-grants-1978_03
ORD IDord-031502b4dac8484e8460f750022bf05b
Source noteuspto-grants-1978_03