HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-dimethylamino-N-[3,4-dichlorotolyl]-cyclohexane carboxamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 1-dimethylamino-N-[3,4-dichlorotolyl]-cyclohexane carboxamide | HCID 86733844 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-dimethylamino-N-[3,4-dichlorotolyl]-cyclohexane carboxamide hydrochloride | HCID 86733845 | — |
Reaction Steps
1-Dimethylamino-N-[3,4-dichlorotolyl]-cyclohexane carboxamide (0.658 g.,) was dissolved in ethanol (5 ml.) and ethereal hydrogen chloride (10 ml.) was added. The solution was evaporated to leave a colourless oil which was taken up in the minimum volume of acetic acid. Dropwise addition of ether, with scratching and cooling, precipitated the hydrochloride as colourless prisms which was dried over potassium hydroxide in vacuo (0.688 g., m.p. 160°-170°). Recrystallisation from ethanol (addition of ether) afforded 1-dimethylamino-N-[3,4-dichlorotolyl]-cyclohexane carboxamide hydrochloride as white prisms (0.351 g., 48%); m.p. 162°-166° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04049663 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-94e5847119b94d099175b766cf476d27 |
| Source note | uspto-grants-1977_09 |