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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21408Generated: October 25, 2026

Ethyl chloroacetate → 2-Benzylidenehydrazono-3-ethoxycarbonylmethyl-1-methoxycarbonylmethylimidazolidin-4-one

https://huagongshe.com/reaction/21408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroacetateHCID 7751—
ReactantSodium hydrideHCID 24758—
Reactant2-Benzylidenehydrazono-1-methoxycarbonylmethylimidazolidin-4-oneHCID 136040605—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Product2-Benzylidenehydrazono-3-ethoxycarbonylmethyl-1-methoxycarbonylmethylimidazolidin-4-oneHCID 5412072144.4%

Reaction Conditions

Temperature30 °C

Reaction Steps

In 20 ml of dimethylformamide (DMF) was suspended 96 mg of 60% sodium hydride under ice-cooling, 5 ml of a DMF solution of 548 mg of 2-benzylidenehydrazono-1-methoxycarbonylmethylimidazolidin-4-one was gradually added to the suspension. After stirring the mixture for one hour at 30° C., 254 mg of ethyl chloroacetate was gradually added dropwise thereto, followed by stirring for one hour at 80° C. After cooling the reaction mixture, water and chloroform was added thereto to distribute the mixture between water and chloroform, and the aqueous layer was further extracted three times with chloroform. The organic layer was combined with the extract, the mixture was dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and the residue formed was recrystallized from a mixture of chloroform and n-hexane to obtain 320 mg of 2-benzylidenehydrazono-3-ethoxycarbonylmethyl-1-methoxycarbonylmethylimidazolidin-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05422360
Source datasetuspto-grants-1995_06
ORD IDord-95f5bb33bf7440c88b09193ba4fb2a51
Source noteuspto-grants-1995_06