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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1855944생성일: 2026년 10월 26일

p-Toluenesulfonic acid → cis-4-Tetrahydropyranyloxy 2-cyclopentenol

https://huagongshe.com/reaction/1855944

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물4-Cyclopentene-1,3-diolHCID 278600—
촉매PyridineHCID 1049—
촉매TetrahydrofuranHCID 8028—
용매DichloromethaneHCID 6344—
생성물cis-4-Tetrahydropyranyloxy 2-cyclopentenolHCID 1362325271.7%

반응 단계

To a solution of 5.0 g of 2-cyclopentene-1,4-diol in 300 ml of methylene chloride was added 5 ml of a solution of p-toluenesulfonic acid in tetrahydrofuran (1 millimole/100 ml). A solution of 4.2 g of 2,3-dihydropyran in 30 ml of methylene chloride was then added dropwise with stirring over a period of 1 hour. After stirring overnight at room temperature, 8 drops of pyridine were added. The methylene chloride was evaporated and the residue was dissolved in diethyl ether, washed with water and dried. The residual obtained by evaporating the solvent was chromatographed on silica gel (200 g) using chloroform as an eluent. First, the diether product flowed out. The subsequent effluent was treated in a customary manner to afford 6.6 g of cis-4-tetrahydropyranyloxy 2-cyclopentenol as colorless oily substance boiling at 84° C. (0.7 mmHg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04217284
출처 데이터셋uspto-grants-1980_08
ORD IDord-607412bea2924885b7a1a436db1424ca
출처 메모uspto-grants-1980_08