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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865047Generated: October 30, 2026

Hydrochloric Acid → HCID 57975292, compound

https://huagongshe.com/reaction/1865047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl N-methylaminoacetate hydrochlorideHCID 171173—
Reactant2-(1-Ethoxypropylidene)malononitrileHCID 231470—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductHCID 57975292HCID 5797529266.7%

Reaction Conditions

Temperature15 °C

Reaction Steps

Alternatively the title compound may be prepared by the following procedure. Charge ethanol (3.40 L, denatured with 0.5% toluene) to a 22 L 3-neck reaction flask equipped with a mechanical stirrer, condenser, addition funnel and cooling bath. Cool the ethanol to 8° C. and add sodium ethoxide (805 grams, 11.35 mol) portion-wise over 20 minutes. In a separate flask, combine sarcosine ethyl ester hydrochloride (697 g, 4.54 mol), 2-(1-ethoxy-propylidene)-malononitrile (681 grams, 4.54 mol, prepared in preparation 35) and ethanol (3.0 L) and stir to dissolve the solids. Add the resulting solution to the 22 L flask over 33 minutes while maintaining about 11 C. Maintain the reaction mixture between 10-20° C. for 3.5 hours. Stir the mixture at room temperature overnight, then cool to 1° C. Adjust the pH to 7.0 by adding 1 N HCl (6.58 L) and stir the resulting suspension at 0-5° C. for 3 hours. Collect the precipitate by filtration, rinse the filter cake with deionized water (1.0 L) and vacuum-dry at 40° C., to afford the title compound in 66.7% yield. Mass spectrum (m/e): 222.4 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625932B2
Source datasetuspto-grants-2009_12
ORD IDord-a515ec8926eb496aa1091f8434c7a9e4
Source noteuspto-grants-2009_12