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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77997생성일: 2026년 10월 23일

N-Formylmorpholine → 4-(1,3-Dioxolan-2-yl)benzaldehyde

https://huagongshe.com/ko/reaction/77997

반응식

참여 물질

역할이름HCID투입량
반응물N-FormylmorpholineHCID 20417—
반응물2-(4-Bromophenyl)-1,3-dioxolaneHCID 2773842—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물4-(1,3-Dioxolan-2-yl)benzaldehydeHCID 11829988101.3%

반응 조건

온도-78 °C

반응 단계

To a tetrahydrofuran (100 mL) solution of 2-(4-bromo-phenyl)-1,3-dioxolane (8 g, 34.9 mmol) was added dropwise n-butyl lithium (19.6 mL, 2.67 M hexane solution, 52.4 mmol) at −78° C. After 1 hour of stirring at −78° C., N-formylmorpholine (4.42 g, 38.4 mmol) was added to the mixture, and stirred for 3 hours at the same temperature. This mixture was partitioned into diethyl ether and water. The organic layer was separated, washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (6.3 g). This compound was used in the subsequent reaction without being purified.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841327B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-ebf8b95b75e946869214714f5fd69448
출처 메모uspto-grants-2014_09