HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 86733836, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methylbenzoyl Chloride | HCID 13405 | — |
| Reactant | 1-(Aminomethyl)-N,N-dimethylcyclohexan-1-amine | HCID 2113403 | — |
| Product | HCID 86733836 | HCID 86733836 | — |
Reaction Steps
A solution of p-toluoyl chloride (1 g.) 1-aminomethylcyclohexyl dimethylamine (1 g.) and triethylamine (0.65 g.) in benzene (60 ml.) was heated under reflux for 1.5 hrs. The excess benzene was evaporated under reduced pressure, the residue dissolved in water and extracted with chloroform. The extracts were dried (anhyd. sodium sulphate) and the chloroform evaporated under reduced pressure to give an oil which solidified on cooling. Excess ethereal hydrochloric acid was added to an ethereal solution of the solid and the excess ether removed under reduced pressure. The solid residue was crystallised from isopropanol/petroleum ether (80-100) to give 4-methylbenzamido methyl cyclohexyl dimethylamine hydrochloride m.p. 199°-201° (0.7 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04049663 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-f5260c7ff9184a8587b6bfe9fe8644fe |
| Source note | uspto-grants-1977_09 |