HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethanol → 1-(2-Hydroxyethyl)-4-benzamidopiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-4-Piperidylbenzamide | HCID 118120 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 1-(2-Hydroxyethyl)-4-benzamidopiperidine | HCID 20315176 | 62.4% |
Reaction Steps
A mixture of 2.04 grams (0.01 mole) of 4-benzamidopiperidine, 1.25 grams (1 equivalent) of 2-bromoethanol and 2.76 grams (4-equivalents) of potassium carbonate were stirred at 100° C in 2 milliliters of methyl ethyl ketone for two hours. The mixture was filtered hot and the inorganic residue was washed well with hot methyl ethyl ketone. The filtrate was evaporated to dryness and the resulting white solid recrystallised from ethyl acetate to give 1.55 grams (62%) of 1-(2-hydroxyethyl)-4-benzamidopiperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04024147 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-fd9b453785aa4a6e8795d4b26842388e |
| Source note | uspto-grants-1977_05 |