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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2113659생성일: 2026년 10월 26일

Allyl iodide → 2-allyl-2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenone

https://huagongshe.com/reaction/2113659

반응식

참여 물질

역할이름HCID투입량
반응물Allyl iodideHCID 11166—
반응물Sodium hydrideHCID 24758—
반응물2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenoneHCID 58604073—
용매DimethylformamideHCID 6228—
생성물2-allyl-2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenoneHCID 58604046—

반응 조건

온도2.5 °C

반응 단계

NaH (0.32 g of a 60% dispersion in mineral oil, 8.0 mmol) was added to an ice-cold solution of 2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenone (1.55 g, 6.7 mmol) in anhydrous DMF (30 mL). The mixture was purged with N2 and stirred at 0-5° C. for 45 minutes. Allyl iodide (0.91 mL, 10.0 mmol) was added and, after a few minutes, the cooling bath was removed and the mixture was stirred overnight at room temperature. Additional NaH (0.16 g of a 61.1% dispersion in mineral oil, 4.1 mmol) was added and the mixture was stirred at room temperature for 15 minutes. Allyl iodide (0.46 mL, 5.0 mmol) was added and the mixture was stirred at room temperature for 24 hours. The mixture was partitioned between EtOAc and water, and the aqueous phase was back-extracted with several portions of EtOAc. The combined organics were washed with brine, dried over MgSO4, filtered, and concentrated under vacuum. The residue was purified by Biotage™ (Charlottesville, Va.) flash chromatography on a 40M (4×15 cm) silica gel column, eluting with 1% to 4% EtOAc in hexane, to afford 2-allyl-2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenone as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07432284B2
출처 데이터셋uspto-grants-2008_10
ORD IDord-4ffa97b3f8e743c692bc0288aacb38db
출처 메모uspto-grants-2008_10