HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloropyridine → 4-Methoxybenzyl-2-chloropyridinium hexafluoroantimonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloropyridine | HCID 7977 | — |
| Reactant | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Reactant | Sodium hexafluoroantimonate | HCID 16689647 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Methoxybenzyl-2-chloropyridinium hexafluoroantimonate | HCID 16705392 | — |
Reaction Steps
4,698 g (0.03 mol) of 4-methoxybenzyl chloride and 10.22 g (0.09 mol) of 2-chloropyridine were reacted in 40 ml of methanol at 40° C. for 3 days. After the reaction, the solvent was evaporate in vacuo and ether-water was added to the residue to extract unreacted reactants in the etherial layer. To the aqueous layer containing the pyridinium chloride was added 7.764 g (0.03 mol) of sodium hexafluoroantimonate. The resulting crystals were suction filtered, washed and dried to give the title compound melting at 122°-124° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05070161 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-673c9175f8d040c08ae4b10c9e5a3886 |
| Source note | uspto-grants-1991_12 |