HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → 1-Acetyl-2-n-butoxypiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | 1-Acetylpiperidine | HCID 12058 | — |
| Catalyst | Tetramethylammonium tetrafluoroborate | HCID 12621 | — |
| Product | 1-Acetyl-2-n-butoxypiperidine | HCID 21322866 | 57.1% |
Reaction Steps
In the same manner as indicated in Example 6 there are electrolyzed 8.5 g of N-acetylpiperidine and 49.7 g of n-butanol in the presence of 0.3 g of tetramethylammonium tetrafluoroborate as conducting salt. After throughput of 2.5 Faraday per mol of N-acetylpiperidine the current is switched off. The calculated mean cell voltage is 91 volts. Work-up of the electrolysis solution gives 7.6 g of 1-acetyl-2-n-butoxypiperidine (boiling point 70° C./0.1 mbar; nD25 =1.4656), which corresponds to a product yield of 56.8% and a current efficiency of 45.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04149941 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-9b9a98bbfd09486b8dd6a08cb7fdef27 |
| Source note | uspto-grants-1979_04 |