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HRID 1006308作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Sodium SulfiteHCID 24437—
反応物(+)-NootkatoneHCID 1268142—
反応物Potassium hydroxy sulfiteHCID 23707502—
触媒Osmium TetroxideHCID 30318—
溶媒DimethylformamideHCID 6228—
生成物(4S, 4aR, 6R)-6-Acetyl-4,4a-dimethyl-4,4a,5,6,7,8-hexahydro-3H-naphthalen-2-oneHCID 6991911560%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06787671B2
出典データセットuspto-grants-2004_09
ORD IDord-0be4f6fe76994d19a55261015af85dca
出典メモuspto-grants-2004_09