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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 221917생성일: 2026년 10월 26일

Dimethylformamide → 5-Bromo-2-fluoro-4-(hydroxymethyl)benzaldehyde

https://huagongshe.com/reaction/221917

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Ammonium ChlorideHCID 25517—
반응물2-Bromo-5-fluorobenzyl alcoholHCID 2773349—
반응물1,2,2,3-TetramethylpiperidineHCID 18761772—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물5-Bromo-2-fluoro-4-(hydroxymethyl)benzaldehydeHCID 59278930106.7%

반응 조건

온도-78 °C

반응 단계

Tetramethylpiperidine (0.68 g, 4.87 mmol) was dissolved in tetrahydrofuran (4.5 mL). To the resultant solution was added n-butyllithium (1.0 M n-hexane solution, 4.88 mL) at 0° C., and the solution was then stirred for 15 minutes. The solution was cooled to −78° C., and a solution of (2-bromo-5-fluorophenyl)-methanol (0.50 g, 2.43 mmol) in tetrahydrofuran (2.5 mL) was added dropwise. The temperature of the solution was raised over 2 hours to −40° C. The solution was again cooled to −78° C., and N,N-dimethylformamide (0.47 mL, 6.07 mmol) was added thereto. The temperature of the solution was raised to room temperature, and the solution was then stirred for 30 minutes. Saturated aqueous ammonium chloride was added, and the resultant mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and then concentrated under reduced pressure, to thereby obtain the titled compound (604.3 mg, quantitative).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207134B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-f40641d84fb74929ad904fe03f5c0e41
출처 메모uspto-grants-2012_06