Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 98961-87-6 | HCID 86593856 | 95% |
Reaction Steps
392.1 g of anhydrous methanesulfonic acid were added dropwise to 340.8 g of piperidine in 700 ml of isopropanol while stirring and cooling with water over the course of one hour, during which the temperature rose to 75° C. The dropping funnel was washed with 50 ml of isopropanol, and the mixture was then cooled to 25° C. and stirred at this temperature for half an hour. The precipitated product was filtered off with suction, washed twice with 200 ml of diisopropyl ether each time and dried at 50° C. in vacuo. 688.9 g of piperidinium methanesulfonate were obtained as colorless crystals; which is 95% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06835839B2 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-a4b440c647844ae3b503108f43f38c81 |
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| Source note | uspto-grants-2004_12 |
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