Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | 4-Methoxy-[1,3]dioxolo[4,5-g]isoquinoline | HCID 21336 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 14820228 | HCID 14820228 | 100% |
Reaction Steps
8-Methoxy-6,7-methylenedioxyisoquinoline (5) in an amount of 2.03 g (10 mmol) was dissolved into 40 ml of toluene while heating them at 60° C. Then, 1.13 ml (12 mmol) of dimethyl sulfate was added and stirred at 60° C. for 4 hours. After cooling, deposited crystals were collected by filtration, washed with toluene and then dried to obtain 3.30 g of 8-methoxy-2-methyl-6,7-methylenedioxyisoquinolinium methyl sulfate (6) with a yield of 100%. The resultant product was then recrystallized from ethanol: m.p. 172°-4° C. IR and NMR of the resultant product are listed below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04963684 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-784a469d1379470badc29c16ff04ad27 |
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| Source note | uspto-grants-1990_10 |
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