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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485983Generated: October 25, 2026

Ammonia → p-(1-Trifluoromethyl-heptyloxy)-benzamidine hydrochloride

https://huagongshe.com/reaction/485983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
Reactantp-(1-Trifluoromethyl-heptyloxy)-benzonitrileHCID 15724839—
SolventEthanolHCID 702—
Productp-(1-Trifluoromethyl-heptyloxy)-benzamidine hydrochlorideHCID 19097075—

Reaction Steps

Into 20 ml of dry ethanol containing 3.76 g of oa p-(1-trifluoromethyl-heptyloxy)-benzonitrile, about 1 g of dry hydrogen chloride was introduced under stirring at a temperature below 10° C. After stirring at room temperature for 3 days, solvent was distilled off to obtain any oily product To this, were added slowly 20 ml of dry ethanol containing about 2 g of ammonia under cooling with ice, followed by stirring at room temperature for 3 days. Ethanol and ammonia were removed to obtain 3.40 g of oily oa p-(1-trifluoromethyl-heptyloxy)-benzamidine hydrochloride. This oily hydrochloride was solidified by trituration in hexane to use the following reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05290478
Source datasetuspto-grants-1994_03
ORD IDord-7627d80200ea4da09ca22f0df1c755ee
Source noteuspto-grants-1994_03