Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 13472770 | HCID 13472770 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13472771 | HCID 13472771 | — |
Reaction Steps
The organic halide, methyl iodide (5 mL), was added to a solution of 4,5-dimethoxy-1,7,8,12b-tetrahydrobenzo[6,7]cyclohepta[1,2,3-de]isoquinoline (3.0 g, 10 mmol; described in example 2) in acetone (75 mL). The mixture was heated at reflux (reflux time=1 hr.), cooled to 0° C. and diluted with diethyl ether. The solid (isoquinolinium salt) was collected and dried under vacuum to give 4,5-dimethoxy-2-methyl-1,7,8,12b-tetrahydrobenzo[6,7]cyclohepta[1,2,3-de]isoquinolinium iodide, mp 179°-182° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04522946 |
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| Source dataset | uspto-grants-1985_06 |
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| ORD ID | ord-1c78cc734ccb4b8f98911c59b56c3ff4 |
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| Source note | uspto-grants-1985_06 |
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