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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 479603생성일: 2026년 10월 27일

4-Hydroxybenzaldehyde → 4-(2-Tetrahydro-2H-pyranoxy)benzaldehyde

https://huagongshe.com/reaction/479603

반응식

참여 물질

역할이름HCID투입량
반응물4-HydroxybenzaldehydeHCID 126—
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
용매TetrahydrofuranHCID 8028—
생성물4-(2-Tetrahydro-2H-pyranoxy)benzaldehydeHCID 11252736—

반응 단계

40.0 g of 4-hydroxybenzaldehyde are dissolved in 400 ml of abs. THF under a protective-gas atmosphere, 55.1 g of dihydropyran and 13.7 g of pyridinium p-toluenesulfonate are added, and the mixture is stirred overnight at room temperature. The solvent is removed in a rotary evaporator, and the residue is subjected to conventional work-up, giving 4-(tetrahydropyran-2-yloxy)benzaldehyde (“BA”) as a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06645991B1
출처 데이터셋uspto-grants-2003_11
ORD IDord-4c452461370e4d9e8bf9bcf189ef2201
출처 메모uspto-grants-2003_11