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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 852994생성일: 2026년 10월 25일

Dimethylformamide → HCID 58615402, 화합물

https://huagongshe.com/reaction/852994

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물6-Bromo-4-cyclohexylmethoxy-quinolineHCID 58615367—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Ammonium ChlorideHCID 25517—
생성물HCID 58615402HCID 5861540248%

반응 단계

To a solution of 6-bromo-4-cyclohexylmethoxy-quinoline (0.510 g, 1.59 mmol) in THF (10 mL) was added dropwise a 2.5M solution of n-butyllithium in hexanes (0.765 mL, 1.92 mmol, 1.2 equiv.) at −70° C. During the addition, the color of the solution was turned into red and this solution was stirred for 1 h at this temperature. Then, a solution of dimethylformamide (0.246 mL, 3.19 mmol) in THF (1 mL) was added dropwise. After addition, the mixture was allowed to warm to room temperature and stirred for 2 h. Then, the mixture was diluted with saturated ammonium chloride solution and the two layers were separated. The aqueous layer was extracted with ethyl acetate (3×150 mL). The combined organic extracts were washed with brine solution and dried over anhydrous magnesium sulfate. Filtration of the drying agent and removal of the solvent under the vacuum gave the crude residue which was purified by using a Biotage silica gel column chromatography to afford 0.205 g (48% yield) of 4-cyclohexylmethoxy-quinoline-6-carbaldehyde as a white solid: EI-HRMS m/e calcd for C17H19NO2 (M+) 269.3513, found 269.3511.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07253285B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-a6c85ebe63f7402ca130200f336997fb
출처 메모uspto-grants-2007_08