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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Dimethylacetamide | HCID 31374 | — |
| 반응물 | p-(Dimethoxymethyl)anisole | HCID 75140 | — |
| 생성물 | (1s,3r,6r,10r)-3-(4'-Methoxyphenyl)-10-hydroxy-2,4,7-trioxabicyclo[4.4.0]decane | HCID 20588607 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06569355B1 |
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| 출처 데이터셋 | uspto-grants-2003_05 |
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| ORD ID | ord-63a9c62168864f38bdd617b0cdcec539 |
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| 출처 메모 | uspto-grants-2003_05 |
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