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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7890생성일: 2026년 10월 25일

Methyl iodide → 4-Bromo-2-butyl-6-fluoro-5-methoxy-1-indanone

https://huagongshe.com/reaction/7890

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium BicarbonateHCID 516892—
반응물4-Bromo-2-butyl-6-fluoro-5-hydroxy-1-indanoneHCID 21990852—
용매DimethylformamideHCID 6228—
생성물4-Bromo-2-butyl-6-fluoro-5-methoxy-1-indanoneHCID 2199090681.6%

반응 단계

A mixture of 4-bromo-2-butyl-6-fluoro-5-hydroxy-1-indanone (2.17 g, 7.23 mmol), N,N-dimethylformamide (14.5 mL), methyl iodide (0.675 mL, 10.84 mmol), and sodium bicarbonate (1.50 g, 18.1 mmol) was stirred at room temperature for 17 hours. The solvent was evaporated under vacuum. The residue in EtOAc (150 mL) was washed with water (5×100 mL) and brine (50 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (2.29 g). The crude product was dissolved in CH2CL2 (5 mL) and the solution filtered through a pad of EM silica gel 60 (20 mL) using an additional 60 mL of CH2Cl2 to elute the silica gel. The CH2Cl2 filtrate was evaporated under vacuum to afford 4-bromo-2-butyl-6-fluoro-5-methoxy-1-indanone (1.86 g) as a pink oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-835f01ea929a484fbdde0611e5ce74b3
출처 메모uspto-grants-2006_08