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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78050생성일: 2026년 10월 24일

N-Formylmorpholine → 4-(Phenoxymethyl)benzaldehyde

https://huagongshe.com/ko/reaction/78050

반응식

참여 물질

역할이름HCID투입량
반응물N-FormylmorpholineHCID 20417—
반응물1-Bromo-4-(phenoxymethyl)benzeneHCID 726149—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물4-(Phenoxymethyl)benzaldehydeHCID 12106287100.6%

반응 조건

온도-78 °C

반응 단계

To a tetrahydrofuran solution (50 mL) of 1-bromo-4-phenoxymethyl-benzene (4.69 g, 17.8 mmol) described in Manufacturing Example 86-1-1 was added dropwise n-butyl lithium (16.8 mL, 1.59 M hexane solution, 26.7 mmol) at −78° C. After 40 minutes of stirring at −78° C., N-formylmorpholine (2.25 g, 19.6 mmol) was added to this mixture, which was then stirred for a further 30 minutes at that 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 (3.8 g). This compound was used in the subsequent reaction without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841327B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-e216d7ae9146476abe7f5177d0c58919
출처 메모uspto-grants-2014_09