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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 495319생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/495319

반응식

참여 물질

역할이름HCID투입량
반응물4-HydroxybenzaldehydeHCID 126—
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
용매DichloromethaneHCID 6344—
생성물4-(2-Tetrahydro-2H-pyranoxy)benzaldehydeHCID 1125273687%

반응 단계

4-Hydroxybenzaldehyde (43.4 g, 0.355 mol), dihydropyran (44.4 ml, 0.495 mol), pyridinium p-toluenesulphonate (11.6 g, 0.046 mol, 0.1 mol equiv.) and dichloromethane (300 ml) were stirred for 16 h at room temperature. The mixture was washed with dilute aqueous sodium hydroxide solution (2×300 ml), water (200 ml), brine (300 ml), and finally with water (250 ml), dried over sodium sulphate and evaporated to dryness to leave a dark brown oil(63 g, 87%). This was used without further purification in the following step 1CW02. 1H NMR showed expected signals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06939479B2
출처 데이터셋uspto-grants-2005_09
ORD IDord-a876761294254d60891a607502043b2f
출처 메모uspto-grants-2005_09