HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1-Benzyl-2,6-diethyl-2,3,6-trimethyl-4-benzamidopiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(2,6-Diethyl-2,3,6-trimethylpiperidin-4-yl)benzamide | HCID 22486017 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sulfolane | HCID 31347 | — |
| Product | 1-Benzyl-2,6-diethyl-2,3,6-trimethyl-4-benzamidopiperidine | HCID 20348330 | — |
Reaction Steps
20 g of 2,6-diethyl-2,3,6-trimethyl-4-benzamidopiperidine (compound no. 9), 12.5 g of benzylbromide, 1 g of potassium iodide and 20 g of potassium carbonate are stirred in 200 ml of tetrahydrothiophene dioxide (sulpholane) at 110° C. for 4 days. Thereafter the reaction mixture is diluted with 200 ml of toluene, cooled to room temperature and purified by filtration. The filtrate is washed four times with about 200 ml of water, the toluene phase is dried over sodium sulfate and evaporated under vacuum. Crystallization of the residue from acetic acid ethyl ester yields 1-benzyl-2,6-diethyl-2,3,6-trimethyl-4-benzamidopiperidine (compound no. 48); m.p. 234°-236° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04191683 |
| Source dataset | uspto-grants-1980_03 |
| ORD ID | ord-b3576292e75e412ab03c0bf3c6f01fdc |
| Source note | uspto-grants-1980_03 |