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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6072Generated: October 26, 2026

Hydrochloric Acid → Ethyl 4-[5-(2-methoxyphenoxy)pentoxy]benzenecarboximidate hydrochloride

https://huagongshe.com/reaction/6072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
Reactant4-[5-(2-Methoxyphenoxy)pentoxy]benzonitrileHCID 19794885—
SolventDiethyl EtherHCID 3283—
ProductEthyl 4-[5-(2-methoxyphenoxy)pentoxy]benzenecarboximidate hydrochlorideHCID 19794923—

Reaction Conditions

Temperature5 °C

Reaction Steps

Ethanol (2 B anhydrous, 16.5 L) is cooled with an ice-salt bath to 0° C. Anhydrous hydrogen chloride is introduced until the solution is saturated (~8 hours). At this time the internal temperature is 5° C. To this is added 4-[5-(2-methoxyphenoxy)pentoxy]benzonitrile (1.64 kg, 5.26 mol) as a solid within a period of 10 minutes. At this point additional hydrogen chloride is introduced to maintain saturation at 5° C. for another 8 hours. Almost complete solution is achieved and the color is yellow. The reaction mixture is stirred for a total of 84 hours and the temperature range maintained is 5°-10° C. The resulting slurry is diluted with diethyl ether (52 L) to complete precipitation. The slurry is stirred for 1 hours and filtered. The filter cake is washed with diethyl ether (3×4 L) and air-dried for 1/2 hour to yield ethyl 4-[5-(2-methoxyphenoxy)pentoxy]benzenecarboximidate hydrochloride which is used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246965
Source datasetuspto-grants-1993_09
ORD IDord-47447b95a1bf45f4834161d3ef59f534
Source noteuspto-grants-1993_09