HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → HCID 54214416, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-Methylhomoveratrylamine | HCID 77039 | — |
| Reactant | AC1Ogrol | HCID 7173934 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54214416 | HCID 54214416 | — |
Reaction Steps
A solution of 10.93 g (0.056 mol) of N-methylhomoveratrylamine in 50 ml of abs. dimethylformamide was treated at 5° with 15.7 g of potassium carbonate and 13.6 g (0.056 mol) of (R)-(-)-3-benzyloxy-2-methylpropyl bromide [Helv. Chim. Acta 60, 940, (1977)]. The mixture was stirred at room temperature for 18 hours and then evaporated under reduced pressure. The residue was taken up in a mixture of water and ethyl acetate. The organic extracts were dried over magnesium sulphate and evaporated under reduced pressure. The residue was distilled at 218°/260 Pa. The N-[(S)-3-(benzyloxy)-2-methylpropyl]-3,4-dimethoxy-N-methylphenethylamine, which was obtained as a colourless oil, was used directly in the next step. [α]D ;20 =+7.3° (c=1, ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05302727 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-55f3e6c866d3451f9e8abc0891e81c15 |
| Source note | uspto-grants-1994_04 |