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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 374482생성일: 2026년 10월 24일

4-Hydroxybenzaldehyde → (R)-(-)-4-(oxiranylmethoxy)-benzaldehyde

https://huagongshe.com/ko/reaction/374482

반응식

참여 물질

역할이름HCID투입량
반응물4-HydroxybenzaldehydeHCID 126—
반응물Potassium CarbonateHCID 11430—
반응물Benzenesulfonic acid, 3-nitro-, (2R)-2-oxiranylmethyl esterHCID 146513—
용매Methyl Ethyl KetoneHCID 6569—
생성물(R)-(-)-4-(oxiranylmethoxy)-benzaldehydeHCID 703749889.1%

반응 단계

In 800 ml of anhydrous methyl ethyl ketone was dissolved 23.54 g of 4-hydroxybenzaldehyde and 50 g of (R)-(-)-glycidyl m-nitrobenzenesulfonate. To the solution was added 34.6 g of anhydrous potassium carbonate, and the mixture was refluxed with heating for 2.5 hours. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was extracted with ethyl acetate. The extract was washed with water, dried with magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and purified with chloroform to give 30.6 g of the title compound (yield 89%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05480899
출처 데이터셋uspto-grants-1996_01
ORD IDord-0142865354294b02b38cff5746f2279e
출처 메모uspto-grants-1996_01