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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1887418생성일: 2026년 10월 27일

3,4-dihydro-2H-pyran → 2-But-3-enoxyoxane

https://huagongshe.com/reaction/1887418

반응식

참여 물질

역할이름HCID투입량
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물3-Buten-1-olHCID 69389—
반응물Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
용매DichloromethaneHCID 6344—
생성물2-But-3-enoxyoxaneHCID 31994589%

반응 단계

In a 1000 ml rb flask were placed 3-buten-1-ol (7.21 g, 100.00 mmol), 3,4-dihydro-2H-pyran (12.62 g, 150.00 mmol) and pyridinium p-toluenesulfonate (2.51 g, 10.00 mmol) in 350 ml of anhydrous dichloromethane. The reaction mixture was stirred at room temperature for 4 h. Then the reaction mixture was concentrated and the residue was purified by column with Hexane/Ethyl acetate=100/5 to provide 13.90 g of the desired product as an oil (89.0%). 1H-NMR (DMSO-d6) δ 5.851-5.742 (m, 1H), 5.103-5.011 (d, 1H), 4.997-4.985 (d, 1H), 4.555-4.537 (t, 1H), 3.745-3.611 (m, 2H), 3.433-3.347 (m, 2H), 2.290-2.236 (m, 2H), 1.698-1.675 (m, 2H), 1.611-1.566 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501755B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-b9887947d73e43e8bac1958882e96144
출처 메모uspto-grants-2013_08