HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-Methyl-6,7-dimethoxy-1[4,5,6-triethoxy-7-nitro-3-phthalidyl]-1,2,3,4-tetrahydro-isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6,7-Dimethoxy-2-methyl-3,4-dihydroisoquinolin-2-ium iodide | HCID 2826990 | — |
| Reactant | 4,5,6-Triethoxy-7-nitrophthalide | HCID 6452177 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methyl-6,7-dimethoxy-1[4,5,6-triethoxy-7-nitro-3-phthalidyl]-1,2,3,4-tetrahydro-isoquinoline | HCID 20560980 | — |
Reaction Steps
200 g (0.6 mole) of 2-methyl-6,7-dimethoxy-3,4-dihydro-isoquinolinium iodide (prepared in the same manner as the compound of Example A) 186 g of 4,5,6-triethoxy-7-nitrophthalide and 100 g of potassium carbonate are added to 1.5 l of methanol while stirring. The reaction mixture is stirred for 24 hours at a temperature below the boiling point of the solvent, and is then allowed to cool; 900 ml of water is added and the reaction solution is allowed to crystallise. The solution is filtered, rinsed with methanol, and then with water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04302458 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-bc17c10b4dd148d4aaee83389a8f65d7 |
| Source note | uspto-grants-1981_11 |