HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 1-Methoxypiperidin-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-Methoxypiperidin-4-one | HCID 19936653 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Methoxypiperidin-4-ol | HCID 3022606 | 89.8% |
Reaction Steps
Under an atmosphere of argon, 200 ml ethanol was cooled to 10° C. and 3.7 g sodium borohydride was added. A solution of 25 g 1-methoxy-piperidin-4-one (prepared according to J. Org. Chem. 1961, 26, 1867-74) in 200 ml ethanol was added to the stirred suspension, while the temperature was kept in the range of 15-20° C. Then the mixture was stirred at ambient temperature for 3 hours. 50 ml aqueous ammonium chloride was added slowly and then the solvent evaporated. The residue was purified by chromatography on silica gel, using ethyl acetate as a solvent. Thus, 22.8 g 1-methoxy-piperidin-4-ol was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08574607B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-ee4279eae629444bacc75cdd21ca8e1d |
| Source note | uspto-grants-2013_11 |