HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-[3-(3-Hydroxyphenyl)-piperidino]ethanol hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Phenol, 3-(3-piperidinyl)- | HCID 12937950 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-[3-(3-Hydroxyphenyl)-piperidino]ethanol hydrochloride | HCID 23045621 | 41% |
Reaction Conditions
| Temperature | -30 °C |
|---|
Reaction Steps
Ethylenoxide (0.36 ml, 7.0 mmol) was added to a stirred solution of 3-(3-hydroxyphenyl)piperidine (1.0 g, 5.6 mmol) in methanol (150 ml), maintaining the temperature at -30° C., whereafter the reaction mixture was allowed to reach room temperature. (The reaction was followed by TLC). More ethylenoxide (0.5 ml, 9.8 mmol) was added in portions until the reaction was complete (two weeks). An excess of ethereal hydrogen chloride was added and the solvent was evaporated. The oily residue was passed through a silica column with 10% methanol in chloroform. After evaporation the hydrochloride was recrystallized from ethanol/ether to yield 0.6 g (41%) of 2-[3-(3-hydroxyphenyl)-piperidino]ethanol hydrochloride, m.p. 116.5°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04937346 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-437a9ef14ac14818ac1a8a0d919bd46e |
| Source note | uspto-grants-1990_06 |