HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → tert-Butyl 4-(1-hydroxyethyl)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester | HCID 10987983 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl 4-(1-hydroxyethyl)piperidine-1-carboxylate | HCID 21989903 | 96.6% |
Reaction Steps
To a solution of 0.400 g (1.76 mmol) of 4-acetyl-piperidine-1-carboxylic acid tert-butyl ester in ethanol (3 mL) is added 0.134 g (3.52 mmol) of sodium borohydride. The mixture is stirred at room temperature for 1 hour then a saturated aqueous solution of ammonium chloride is added to consume excess reactants. The mixture is washed with ethyl acetate and the combined organic phase is dried over anhydrous sodium sulfate and concentrated under reduced pressure to provide 0.390 g (96.6%) of 4-(1-hydroxy-ethyl)-piperidine-1-carboxylic acid tert-butyl ester as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952004B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-a8f3e6c1c76f4cb0b106e7c11f4099d4 |
| Source note | uspto-grants-2015_02 |