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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 652114생성일: 2026년 10월 24일

p-Toluenesulfonic acid → 4-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-ol

https://huagongshe.com/ko/reaction/652114

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물2-Butyne-1,4-diolHCID 8066—
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물TriethylamineHCID 8471—
용매TetrahydrofuranHCID 8028—
생성물4-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-olHCID 11123315—

반응 단계

To a solution of 90 g (1.07 mol) of 2-butyne-1,4-diol and 9 g of p-toluenesulfonic acid in 1000 ml of tetrahydrofuran, cooled to 0° C., there were added dropwise 104.88 ml (96.69 g, 1.15 mol) of dihydropyran, and thereafter the reaction mixture was stirred for 3 hours at room temperature. It was then neutralized with triethylamine and evaporated in vacuo. The residue was purified by silica gel column chromatography (2000 g) using hexane-ethyl acetate (80:20) as eluant, to yield 2-butyne-1,4-diol monotetrahydropyranyl ether and a small amount of the bis-tetrahydropuranyl ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04670465
출처 데이터셋uspto-grants-1987_06
ORD IDord-cf7836657d394dc5b655d8618611ccb7
출처 메모uspto-grants-1987_06