HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-Methyl-6,7,8-trimethoxy-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 | 4,5,6-Triethoxy-7-nitrophthalide | HCID 6452177 | — |
| Reactant | 2-Methyl-6,7,8-trimethoxy-3,4-dihydro-isoquinolinium iodide | HCID 12899014 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methyl-6,7,8-trimethoxy-1[4,5,6-triethoxy-7-nitro-3-phthalidyl]-1,2,3,4-tetrahydro-isoquinoline | HCID 12800935 | — |
Reaction Steps
235 g (0.647 mole) of 2-methyl-6,7,8-trimethoxy-3,4-dihydro-isoquinolinium iodide (described in J. Chem. Soc. 1951, 1150), 201.4 g of 4,5,6-triethoxy-7-nitrophthalide and 107 g of potassium carbonate are added to 1.240 liters of methanol. After stirring for 24 hours at a temperature below the boiling point of the solvent, 730 ml of water is added and the reaction solution is allowed to crystallise. The crystals are collected by filtration, washed with water and dried, providing 270 g of C27H34O10N2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04302458 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-d0b3c160f2e54b30ab7966eec3e733a8 |
| Source note | uspto-grants-1981_11 |