HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-2-ethyl-cyclohexylamino-3,4,5-trimethoxy-benzoate hyrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Benzoyl chloride, 3,4,5-trimethoxy- | HCID 78282 | — |
| Reactant | Cyclohexylamino ethanol | HCID 20285879 | — |
| Product | N-2-ethyl-cyclohexylamino-3,4,5-trimethoxy-benzoate hyrochloride | HCID 86734520 | — |
Reaction Steps
2.86 g. of cyclohexylamino ethanol and 2.02 g. of triethyl amine are dissolved in 30 ml. of anhydrous ethyl acetate. A solution of 4.6 g. of 3,4,5-trimethoxybenzoyl-chloride and 20 ml. of anhydrous ethyl acetate are added under stirring and boiling. The reaction mixture is refluxed for 2 hours, whereafter it is cooled and the precipitate is filtered off by suction and washed with ethyl acetate. The ethyl acetate solution is saturated with gaseous hydrochloric acid. The mixture is refluxed for an hour. On cooling white crystals precipitate. Thus N-2-ethyl-cyclohexylamino-3,4,5-trimethoxy-benzoate-hyrochloride is obtained. M.p.: 209° - 210° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04010193 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-eb1b2547ed2e407689cd187d69bedb1f |
| Source note | uspto-grants-1977_03 |