참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 4-Hydroxycyclopent-2-en-1-one | HCID 4169160 | — |
| 촉매 | p-Toluenesulfonic acid | HCID 6101 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-(Tetrahydro-pyran-2-yloxy)-cyclopent-2-enone | HCID 12838010 | 93.7% |
반응 단계
In 300 ml of dichloromethane was dissolved 10 g of 4-hydroxy-2-cyclopentenone. To the solution were added 25.7 g of dihydropyran and 0.5 g of p-toluenesulfonic acid, and the mixture was stirred at room temperature for 45 minutes. The reaction solution was poured into an aqueous solution of sodium hydrogencarbonate. The organic layer was separated. The aqueous layer was further extracted with dichloromethane. The organic layers were combined, washed with a saturated aqueous saline solution, then dried (Na2SO4). The solvent was evaporated off, and the residue was subjected to a silica gel column chromatography, followed by elution with hexane--ethyl acetate (7:3) to give 17.4 g of 4-(2-tetrahydropyranyl)oxy-2-cyclopentenone as an oily product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04851422 |
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| 출처 데이터셋 | uspto-grants-1989_07 |
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| ORD ID | ord-71408589cb3444fbb85df478f0348ffe |
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| 출처 메모 | uspto-grants-1989_07 |
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