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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2113676생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2113676

반응식

참여 물질

역할이름HCID투입량
반응물Butyl iodideHCID 10962—
반응물6-Methoxy-alpha-tetraloneHCID 14112—
반응물Sodium hydrideHCID 24758—
용매TetrahydrofuranHCID 8028—
생성물2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenoneHCID 58604073—

반응 단계

A mixture of 6-methoxy-3,4-dihydro-1(2H)-naphthalenone (400 mg, 2.27 mmol), iodobutane (0.284 mL, 2.5 mmol), NaH (98 mg of a 61.1% dispersion in mineral oil, 2.5 mmol), and anhydrous tetrahydrofuran (THF, 1 mL) was placed under a N2 atmosphere and stirred at room temperature for 15.5 hours. The mixture was partitioned between EtOAc (20 mL) and water (30 mL) containing 2N HCl (3 mL). The organic phase was washed with brine (20 mL), dried over MgSO4, filtered, and evaporated under vacuum to afford an oil. The crude product was purified by preparative layer chromatography on five 0.1×20×20 cm silica gel GF plates (Analtech, Newark, Del.), developing with CH2Cl2. The UV visible product band was eluted with EtOAc and the eluant evaporated under vacuum to provide 2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenone as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07432284B2
출처 데이터셋uspto-grants-2008_10
ORD IDord-7d06554a428c4e888c8f720f297954f1
출처 메모uspto-grants-2008_10