Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | HCID 21516113 | HCID 21516113 | — |
| Product | HCID 86667142 | HCID 86667142 | 93% |
Reaction Steps
Methyl allylsulfonate (21.4 g, 0.157 mol) synthesized by the conventional method and pyridine (13.1 g, 0.166mol, 1.05 eq) were reacted by stirring for 2 hours at 80° C. After completed the reaction, unreacted pyridine was removed under reduced pressure, crude substance was washed with ethyl acetate several times. The desired product of 1-methylpyridinium allylsulfonate (31.4 g, 0.146 mmol, 93% yield) was obtained by drying by heating under reduced pressure. Melting point was 39° C. Measurement result of 1H NMR was shown as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546609B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-6ab08a99bfd345f7b426d8ee3c6236eb |
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| Source note | uspto-grants-2013_10 |
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