HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 22758148, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-(2,3-dihydro-1H-inden-2-yl)ethanol | HCID 10352000 | — |
| Reactant | HCID 22758147 | HCID 22758147 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 22758148 | HCID 22758148 | — |
Reaction Steps
To a solution of 18 gm. (0.057 mole) of p-toluene sulfonic acid, ester with 2-indanethanol in 100 ml. of toluene, 14 cc. (0.143 mole) of piperidine is added. The mixture is refluxed for 11.5 hrs. and treated with 250 ml. of water and 100 ml. of ether. The organic layer is separated, washed with water, dried (MgSO4) and evaporated in vacuo to give a dark colored oil. The oil is treated with ethereal - HCl to give 15.7 gm. (97%) of 1-[2-(2-indanyl)ethyl]piperidine hydrochloride. Crystallization from ethanol-ether gives 11.5 gm. (72%) of product as off-white crystals; m.p. 204.5°-207°, λNujolmax. 2700-2250 cm-1 (--NH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04127578 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-b69425ffa73c4671a425fffa5d549df0 |
| Source note | uspto-grants-1978_11 |