HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1039702Erstellt: 27. Oktober 2026
Water → (R)-tert-butyl 1-fluoro-3,4-dihydroxy-1-phenylbutan-2-ylcarbamate
https://huagongshe.com/reaction/1039702
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | tert-Butanol | HCID 6386 | — |
| Edukt | Sodium Sulfite | HCID 24437 | — |
| Edukt | Methyl morpholine oxide | HCID 82029 | — |
| Edukt | tert-butyl (1S,2R)-1-fluoro-1-phenylbut-3-en-2-ylcarbamate | HCID 86635707 | — |
| Katalysator | Osmium | HCID 23937 | — |
| Produkt | (R)-tert-butyl 1-fluoro-3,4-dihydroxy-1-phenylbutan-2-ylcarbamate | HCID 67270991 | — |
Reaktionsschritte
To a 250 mL RBF containing tert-butyl (1S,2R)-1-fluoro-1-phenylbut-3-en-2-ylcarbamate (105.00 mg, 396 mmol)(mixture of diasteromers at benzylic fluoride stereocenter) was added tert-butanol (3 mL) and water (1 ml). The mixture was allowed to stir at 23° C. for 2 min, then NMO (139 mg, 1187 mmol) and osmium tetraxide (124 μA, 396 mmol) were added and the reaction was allowed to stir for another 48 h. before the reaction was quenched with water and sodium sulfite (1496 mg, 11872 mmol). The reaction was allowed to stir for 15 min and then extracted with EtOAc (3×). The combined organics were washed with HCl (1 N), sodium bicarbonate, brine and dried over sodium sulfate. The dried solution was passed through a plug of silica gel and concentrated to give 102 mg of a colorless oil
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08552181B2 |
|---|
| Quelldatensatz | uspto-grants-2013_10 |
|---|
| ORD ID | ord-fc1aa90153f141789ea0a6c8dcf5e13c |
|---|
| Quellennotiz | uspto-grants-2013_10 |
|---|