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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 606190생성일: 2026년 10월 25일

Dimethylformamide → 3-Tert-butoxy-5-chloropyrazine-2-carboxaldehyde

https://huagongshe.com/reaction/606190

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물2,2,6,6-TetramethylpiperidineHCID 13035—
반응물2-tert-Butoxy-6-chloropyrazineHCID 22248526—
반응물ButyllithiumHCID 178418339—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물3-Tert-butoxy-5-chloropyrazine-2-carboxaldehydeHCID 22248202—

반응 조건

온도-30 °C

반응 단계

After dissolving 11.4 ml of 2,2,6,6-tetramethylpiperidine in 100 ml of tetrahydrofuran, the solution was cooled to −30° C. Next, 24.1 ml of n-butyllithium (2.6 M, n-hexane solution) was added dropwise under a nitrogen atmosphere. After stirring for 5 minutes, the mixture was cooled on ice and stirred for an additional 20 minutes. It was then cooled to −78° C., and a solution of 9.00 g of 2-tert-butoxy-6-chloropyrazine in tetrahydrofuran (10 ml) was added dropwise at below −70° C. The mixture was then stirred for 30 minutes, and 6 ml of N,N-dimethylformamide was added dropwise at below −65° C. After 10 minutes, 50 ml of toluene was added to the reaction solution at below −60° C., and after 2 minutes, a tetrahydrofuran solution (5 ml) containing 2 ml of water was added at below −65° C. After an additional 5 minutes, 60 ml of 50% aqueous acetic acid was added at once, and after 5 minutes, 100 ml of water was added and the temperature was raised to room temperature. The reaction solution was extracted with ethyl acetate, washed with water, a 1N sodium hydroxide solution, water and saturated brine in that order, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 9.39 g of crude 3-tert-butoxy-5-chloropyrazine-2-carboxaldehyde.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07915274B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-c50da62b6e13438eb64bf75f827d933b
출처 메모uspto-grants-2011_03