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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1006308Erstellt: 25. Oktober 2026

Ethyl Acetate → (4S, 4aR, 6R)-6-Acetyl-4,4a-dimethyl-4,4a,5,6,7,8-hexahydro-3H-naphthalen-2-one

https://huagongshe.com/reaction/1006308

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktSodium SulfiteHCID 24437—
Edukt(+)-NootkatoneHCID 1268142—
EduktPotassium hydroxy sulfiteHCID 23707502—
KatalysatorOsmium TetroxideHCID 30318—
LösungsmittelDimethylformamideHCID 6228—
Produkt(4S, 4aR, 6R)-6-Acetyl-4,4a-dimethyl-4,4a,5,6,7,8-hexahydro-3H-naphthalen-2-oneHCID 6991911560%

Reaktionsschritte

Nootkatone (250 mg) was dissolved in DMF (15 mL), and OsO4 (0.14 mL, 2.5% in tBuOH) was added and stirred for 5 min. OXONE (1.40 g) was added in one portion and the reaction had a final volume (18 mL). The reaction was stirred at room temperature for 3 hours or until the solution becomes colorless. This usually marks the completion of the reaction which was verified by TLC or GC. Na2SO3 (3.0 g) was added, to reduce the remaining Os(VIII), and stirred for an additional hour or until solution became dark brown/black. EtOAc was added to extract the products and 1N HCl was used to dissolve the salts. The organic extract was washed with 1N HCl (100 mL×3) and brine (100 mL), dried over Na2SO4, and the solvent was removed under reduced pressure to obtain the crude product. (4S, 4aR, 6R)-6-Acetyl-4,4a-dimethyl-4,4a,5,6,7,8-hexahydro-3H-naphthalen-2-one was obtained in 60% yield after purification by silica gel column chromatography.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06787671B2
Quelldatensatzuspto-grants-2004_09
ORD IDord-0be4f6fe76994d19a55261015af85dca
Quellennotizuspto-grants-2004_09