HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1,3-Dimethyl-4-p-methoxyphenoxy-hexahydroazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 23339238 | HCID 23339238 | — |
| Product | 1,3-Dimethyl-4-p-methoxyphenoxy-hexahydroazepine | HCID 23339274 | — |
Reaction Steps
23.5 g of 1,3-dimethyl-4-p-hydroxyphenoxy-hexahydroazepine are dissolved in 100 ml of absolute ethanol, 200 ml of 0.5 N ethanolic KOH are added, the reaction mixture is stirred for one hour at 20° and evaporated and the residue is taken up in 250 ml of absolute DMF. 12.6 g of dimethyl sulfate are added in portions, while stirring. The mixture is boiled for 2 hours and evaporated and the residue is worked up in the customary manner, giving 1,3-dimethyl-4-p-methoxyphenoxy-hexahydroazepine, 2 oily isomers, Rf 0.36 and 0.55.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04225608 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-6a1bba5d27e84609bc163f19a2093dbc |
| Source note | uspto-grants-1980_09 |