HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → Methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-(2-Ethoxy-2-phenyl-ethenyl)-1-pyrroline tetrafluoroborate | HCID 86736214 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Methanesulfonate | HCID 85257 | — |
| Product | 2-(1-Piperidyl-2-phenylethenyl]-1-pyrroline- | HCID 53678018 | — |
Reaction Steps
Crude 2-[2-(1-piperidyl)-2-phenyl-ethenyl]-1-pyrroline is produced by refluxing for 12 hours the solution of 9.1 g (0.03 mole) of 2-(2-ethoxy-2-phenyl-ethenyl)-1-pyrroline-tetrafluoroborate in 25 ml of piperidine, and processing the reaction mixture analogously to Example 1. By the addition of 2.8 g of methanesulphonic acid to the solution of the crude base in isopropanol, concentration of this solution in the rotary evaporator and recrystallisation of the residue from acetone/hexane, there is obtained 2-[2-(1-piperidyl-2-phenylethenyl]-1-pyrroline-(1:1)-methanesulphonate, m.p. 123°-124°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04130652 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-aecd6f8d4454451f8f5e03adc516ea9d |
| Source note | uspto-grants-1978_12 |