HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 1-(3'-Trifluoromethylbenzoyl)-2-methoxypiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-[3-(Trifluoromethyl)benzoyl]piperidine | HCID 2980140 | — |
| Catalyst | Tetramethylammonium tetrafluoroborate | HCID 12621 | — |
| Product | 1-(3'-Trifluoromethylbenzoyl)-2-methoxypiperidine | HCID 21322855 | 88.2% |
Reaction Steps
In the same manner as in Example 5, there are electrolyzed 13.5 g of 1-(3'-trifluoromethylbenzoyl)-piperidine and 84.1 g of methanol in the presence of 0.11 g of tetramethylammonium tetrafluoroborate as conducting salt. After throughput of 2.5 Faraday per mol of 1-(3'-trifluoromethylbenzoyl)-piperidine the current is switched off. The calculated mean cell voltage is 34.1 volts. Work-up of the electrolysis solution gives 13.3 g of 1-(3'-trifluoromethylbenzoyl)-2-methoxypiperidine (boiling point 75°-80° C./0.2 mm Hg; nD25 =1.4905) are obtained which corresponds to a product yield of 88.2% and a current efficiency of 70.6%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04149941 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-adaef25251024d3cb922b10bf853c6e7 |
| Source note | uspto-grants-1979_04 |