HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-(3-Chloro-4-cyclohexylphenyl)-3-(diethylamino)-1-propanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diethylammonium chloride | HCID 10197650 | — |
| Reactant | 3-Chloro-4-cyclohexylacetophenone | HCID 56975890 | — |
| Product | 1-(3-Chloro-4-cyclohexylphenyl)-3-(diethylamino)-1-propanone | HCID 20316758 | 76.5% |
Reaction Steps
54 g of diethylamine hydrochloride, 100 g of 3-chloro-4-cyclohexyl-acetophenone and 15.1 g of paraformaldehyde in 75 ml of absolute ethanol were heated under reflux for 4 hours in the presence of 1.5 ml of 10 N hydrochloric acid. When the reaction was complete, the solvent was evaporated over a water bath under the vacuum produced by a water-jet pump, and the residue was then recrystallized from acetone. 116 g (a yield of 76.5% of theory) of 3-chloro-4-cyclohexyl-1-(3-diethylamino-1-oxo-propyl)-benzene were obtained; the product had a melting point of 156°-158° C (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04104383 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-0d78a687fb0246c0a8686e63ca04f1e7 |
| Source note | uspto-grants-1978_08 |