Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Fluorine | HCID 24524 | — |
| Product | HCID 14204773 | HCID 14204773 | — |
Reaction Steps
To 40 ml of acetonitrile were added 1.655 g (20.923 mmol) of pyridine and 1,961 g (20.406 mmol) of methanesulfonic acid (i.e., the amount of pyridine was 1,025 times that of methanesulfonic acid in a molar ratio), and the mixture was cooled to -20° C. A mixed gas of fluorine and nitrogen in a volumetric ratio of 1:4 was then introduced to the mixture at a rate of 50 ml/min under stirring. The amount of fluorine gas introduced was 40.0 mmol. After completion of the reaction, the solvent was distilled off, and 3,691 g ¢19.103 mmol) N-fluoropyridinium methanesulfonate was obtained by crystallizing with ether. The yield was
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05336772 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-9e1ea568b7724014aa156cb79aae2239 |
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| Source note | uspto-grants-1994_08 |
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