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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1383041생성일: 2026년 10월 26일

p-Toluenesulfonic acid → 2H-Pyran, tetrahydro-2-(2-iodoethoxy)-

https://huagongshe.com/reaction/1383041

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물Potassium CarbonateHCID 11430—
반응물1-IodoethanolHCID 17859945—
용매Diethyl EtherHCID 3283—
생성물2H-Pyran, tetrahydro-2-(2-iodoethoxy)-HCID 11118662—

반응 단계

Freshly distilled dihydropyran (Aldrich, 59.0 g, 0.7 mol) was added dropwise to a cooled solution of iodoethanol (Aldrich, 98 g, 0.57 mol) in Et2O (1 L) containing 0.1 g of p-toluenesulfonic acid (Eastman). The solution was then stirred for 1 h at 5°. Solid K2CO3 (Mallinckrodt, 5 g) was then added to the reaction mixture and the resulting suspension stirred an additional 1 h at RT. The reaction was then filtered and the remaining solid washed with Et2O (1 L). The organic solutions were combined and concentrated on a rotary evaporator (in a flask washed with 1% NEt3 in H2O). The crude 2-(2-iodoethoxy)tetrahydro-2-H-pyran (100 g, 68.9%) was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04808625
출처 데이터셋uspto-grants-1989_02
ORD IDord-7aa641c3f1c844ac85b5ba92271b12c8
출처 메모uspto-grants-1989_02