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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukttert-ButanolHCID 6386—
EduktSodium SulfiteHCID 24437—
EduktMethyl morpholine oxideHCID 82029—
Edukttert-butyl (1S,2R)-1-fluoro-1-phenylbut-3-en-2-ylcarbamateHCID 86635707—
KatalysatorOsmiumHCID 23937—
Produkt(R)-tert-butyl 1-fluoro-3,4-dihydroxy-1-phenylbutan-2-ylcarbamateHCID 67270991—

Reaktionsbedingungen

Temperatur23 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08552181B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-fc1aa90153f141789ea0a6c8dcf5e13c
Quellennotizuspto-grants-2013_10