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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | N-(4-chloro-alpha,alpha-dimethylbenzyl)-2-(2-dimethylcarbamoyl-phenoxy)acetamide | HCID 18933598 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[2-(4-chloro-alpha,alpha-dimethylbenzylamino) ethoxy]-N,N-dimethylbenzylamine dihydrochloride hemihydrate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05736568 |
|---|
| Source dataset | uspto-grants-1998_04 |
|---|
| ORD ID | ord-76e144322c96464eb60fa8678a5075e5 |
|---|
| Source note | uspto-grants-1998_04 |
|---|