HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl-[2-(3,4-dimethoxy-phenyl)-ethyl]-amine → N-benzyl-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-hydroxy-2-(2-chlorophenyl)ethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl-[2-(3,4-dimethoxy-phenyl)-ethyl]-amine | HCID 200274 | — |
| Reactant | 2-(2-Chlorophenyl)oxirane | HCID 560709 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-benzyl-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-hydroxy-2-(2-chlorophenyl)ethylamine | HCID 21406690 | — |
Reaction Steps
Similarly 2.71 g. (0.01 mol) of N-benzyl-3,4-dimethoxyphenethylamine and 2.33 g. (0.015 mol) of o-chlorostyrene oxide are reacted in methanol to give N-benzyl-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-hydroxy-2-(2-chlorophenyl)ethylamine. The latter is converted to its hydrochloride, which is dissolved in 90 ml. of methanol and hydrogenated over 1 g. of 10% palladium-on-carbon in 10 ml. of ethyl acetate at room temperature for six hours. The reaction mixture is filtered and evaporated in vacuo to leave N-[2-(3,4-dimethoxyphenyl)ethyl]-2-hydroxy-2-(2-chlorophenyl)ethylamine hydrochloride, m.p. 128°-132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04052506 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-c6616287dc0640478f644555b998b863 |
| Source note | uspto-grants-1977_10 |