HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → (2S)-2-amino-4-fluoro-4-methylpentan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (4S)-4-(2-Fluoro-2-methylpropyl)-2-oxazolidinone | HCID 11194496 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (2S)-2-amino-4-fluoro-4-methylpentan-1-ol | HCID 12167160 | — |
Reaction Steps
To a solution of the fluoro derivative (21.0 g) from Step 4 in 90% aqueous ethyl alcohol (216 mL) was added potassium hydroxide (21.9 g). The mixture was heated at reflux for 4 hours and cooled to room temperature. The mixture was then concentrated and co-evaporated with toluene (3×300 mL). The residue was dissolved in dichloromethane (500 mL) and stirred for 0.5 hour. The suspension was filtered through celite and the celite was washed with dichloromethane (3×100 mL). The filtrate was concentrated to dryness to yield (2S)-2-amino-4-fluoro-4-methylpentan-1-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07375134B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-68e05468e53d4fa682aae5f34e402b4a |
| Source note | uspto-grants-2008_05 |