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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 232229생성일: 2026년 10월 26일

3,4-dihydro-2H-pyran → 4-(Tetrahydro-pyran-2-yloxy)-cyclopent-2-enone

https://huagongshe.com/reaction/232229

반응식

참여 물질

역할이름HCID투입량
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물Sodium BicarbonateHCID 516892—
반응물4-Hydroxycyclopent-2-en-1-oneHCID 4169160—
촉매p-Toluenesulfonic acidHCID 6101—
용매DichloromethaneHCID 6344—
생성물4-(Tetrahydro-pyran-2-yloxy)-cyclopent-2-enoneHCID 1283801093.7%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04851422
출처 데이터셋uspto-grants-1989_07
ORD IDord-71408589cb3444fbb85df478f0348ffe
출처 메모uspto-grants-1989_07