HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 20517523, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 20517552 | HCID 20517552 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 20517523 | HCID 20517523 | — |
Reaction Steps
6-(3-Methoxyphenyl)-2,2,4,6-tetramethylmorpholine hydrochloride (1.4 g) was heated under reflux with concentrated hydrobromic acid (20 ml) under nitrogen for 3 h. The dark solution was reduced to small volume under reduced pressure, diluted with water and neutralised with ammonium hydroxide. The product was extracted into dichloromethane, dried over magnesium sulphate and evaporated to an oil which crystallised from toluene. The title base was converted to its hydrobromide salt by treatment in isopropyl alcohol with a solution of hydrogen bromide in dry ether affording the title compound as its hydrobromide (600 mg) mp 216°-217° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04360519 |
| Source dataset | uspto-grants-1982_11 |
| ORD ID | ord-e9d7fe59149a466bbf615eb73ab1109c |
| Source note | uspto-grants-1982_11 |