Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598307Generated: October 25, 2026

Hydrochloric Acid → 2-[2-(4-chloro-alpha,alpha-dimethylbenzylamino) ethoxy]-N,N-dimethylbenzylamine dihydrochloride hemihydrate

https://huagongshe.com/reaction/1598307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBorane;tetrahydrofuranHCID 2723981—
ReactantN-(4-chloro-alpha,alpha-dimethylbenzyl)-2-(2-dimethylcarbamoyl-phenoxy)acetamideHCID 18933598—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-[2-(4-chloro-alpha,alpha-dimethylbenzylamino) ethoxy]-N,N-dimethylbenzylamine dihydrochloride hemihydrateHCID 131720591—

Reaction Steps

A solution of borane/THF (27 ml, 1M solution) was added to a solution of N-(4-chloro-α,α-dimethylbenzyl)-2-(2-dimethylcarbamoylphenoxy)acetamide (2.0 g) in THF (20 ml) at 0° C. with stirring under a nitrogen atmosphere. The mixture was warmed to ambient temperature and then boiled under reflux for 1 hour. The mixture was evaporated to dryness and 2M hydrochloric acid (50 ml) was added carefully. The mixture was heated on a steam bath for 2 hours, then cooled, washed with ethyl acetate, basified with 2M sodium hydroxide solution and extracted into dichloromethane to give an oil which was distilled under high vacuum to give an oil, b.p. 150° C. at 0.13 mbar. The oil was dissolved in ether and acidified with ethereal hydrogen chloride. The precipitate was collected by filtration to give 2-[2-(4-chloro-α,α-dimethylbenzylamino) ethoxy]-N,N-dimethylbenzylamine dihydrochloride hemihydrate m.p. 140° C. (with effervescence).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736568
Source datasetuspto-grants-1998_04
ORD IDord-76e144322c96464eb60fa8678a5075e5
Source noteuspto-grants-1998_04