HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → Benzyl 4-methyl-2-piperidinecarboxylate p-toluenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 4-Methylpiperidine-2-carboxylic acid hydrochloride | HCID 21988512 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Benzyl 4-methyl-2-piperidinecarboxylate p-toluenesulfonate | HCID 22754709 | 22% |
Reaction Steps
A solution of 20 g (0.112 mole) of 4-methyl-2-piperidinecarboxylic acid hydrochloride, 24 g (0.224 mole) of benzyl alcohol and 25.6 g (0.134 mole) of p-toluenesulfonic acid monohydrate in 100 ml of benzene was refluxed for 5 hours with the continuous removal of water through a Dean-Stark water trap. At the end of this period, the solvent was distilled off, and the residue was washed with ether-n-hexane and recrystallized to give 10 g (22%) of benzyl 4-methyl-2-piperidinecarboxylate p-toluenesulfonate, M.P. 160°-163° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04073913 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-817f02fbe2b040f2b42b253aac7eb65a |
| Source note | uspto-grants-1978_02 |