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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 413609생성일: 2026년 10월 24일

p-Toluenesulfonic acid → (1s,3r,6r,10r)-3-(4'-Methoxyphenyl)-10-hydroxy-2,4,7-trioxabicyclo[4.4.0]decane

https://huagongshe.com/ko/reaction/413609

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물DimethylacetamideHCID 31374—
반응물p-(Dimethoxymethyl)anisoleHCID 75140—
생성물(1s,3r,6r,10r)-3-(4'-Methoxyphenyl)-10-hydroxy-2,4,7-trioxabicyclo[4.4.0]decaneHCID 20588607—

반응 조건

온도62.5 °C

반응 단계

5.0 g (33.8 mmol) of 2 and 8.30 g (45.8 mmol) of p-methoxybenzaldehyde dimethyl acetal were dissolved in 50 ml of anhydrous DMA, and a catalytic amount of 4-toluenesulfonic acid was added until the mixture was acidic. The reaction solution was agitated for about 5 hours in a rotary evaporator at 60-65° C. and a reduced pressure of 30 mbar. The reaction solution was neutralized using triethylamine. 300 ml of ethyl acetate were added, and the mixture was extracted three times with water. The organic phase was dried over Na2SO4, the drying agent was filtered off, and the residue was evaporated under reduced pressure. The crude product was dissolved in a little ethyl acetate, precipitated using n-hexane, filtered off with suction and dried under reduced pressure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06569355B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-63a9c62168864f38bdd617b0cdcec539
출처 메모uspto-grants-2003_05