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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 452558생성일: 2026년 10월 27일

Diisopropylamine → 1-Bromo-4-(4-bromophenyl)-3-(4-methoxyphenyl)butan-2-one

https://huagongshe.com/reaction/452558

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물Phenyltrimethylammonium bromide dibromideHCID 17977687—
반응물4-(4-Bromophenyl)-3-(4-methoxyphenyl)butan-2-oneHCID 66923703—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-Bromo-4-(4-bromophenyl)-3-(4-methoxyphenyl)butan-2-oneHCID 8665084782.8%

반응 조건

온도-78 °C

반응 단계

Diisopropylamine (0.084 g, 0.83 mmol) was dissolved in anhydrous diethyl ether (7.5 mL) under argon atmosphere and cooled to −78° C. BuLi (0.52 mL, 0.83 mmol) was added dropwise to the solution and the resulting solution was allowed to warm to 0° C. for 10 min, then recooled to −78° C. TMS-Cl (freshly distilled over calcium hydride, 0.11 mL, 0.83 mmol) was added dropwise to the solution at −78° C., after addition, the reaction was allowed to stir for an additional 10 min. The solution was then cooled to −90° C., and 4-(4-bromophenyl)-3-(4-methoxyphenyl)butan-2-one (0.25 g, 0.75 mmol) was added dropwise as a solution in anhydrous diethyl ether. After addition was complete, the solution was allowed to stir for an additional 40 min. The reaction was then warmed to 0° C. and phenyltrimethylammonium tribromide (0.31 mg, 0.83 mmol) was slowly added dropwise as a solution in anhydrous THF (4 mL). The resulting solution was allowed to stir at 25° C. for 1 hour. The mixture was diluted with EtOAc and water, washed with NaCl (×3), dried over sodium sulfate and concentrated in vacuo. The crude product was purified using silica gel chromatography (0-30% EtOAc in hexanes gradient) to afford 256 mg of 1-bromo-4-(4-bromophenyl)-3-(4-methoxyphenyl)butan-2-one as a viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492387B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-e34228de24764d1881609c1a56dad532
출처 메모uspto-grants-2013_07