HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 1-Benzoyl-2-methyl-6-methoxypiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | N-Benzoyl-2-methylpiperidine | HCID 275047 | — |
| Catalyst | Tetramethylammonium tetrafluoroborate | HCID 12621 | — |
| Product | 1-Benzoyl-2-methyl-6-methoxypiperidine | HCID 21322854 | 77.6% |
Reaction Steps
In the same manner as in Example 5, there are electrolyzed 43.8 g of 1-benzoyl-2-methylpiperidine and 60.2 g of methanol in the presence of 0.3 g of tetramethylammonium tetrafluoroborate as conducting salt. After throughput of 2.5 Faraday per mol of 1-benzoyl-2-methylpiperidine the current is switched off. After work-up of the electrolysis solution, 39.0 g of 1-benzoyl-2-methyl-6-methoxypiperidine (boiling point 78°-81° C./0.1 mm Hg; nD25 =1.5340) are obtained which corresponds to a product yield of 77.5% and a current efficiency of 62.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04149941 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-bfde8daec3d34f83be4c725b8a450688 |
| Source note | uspto-grants-1979_04 |