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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84240생성일: 2026년 10월 24일

3,4-dihydro-2H-pyran → 2-(4-bromo-3-fluorophenoxy)tetrahydro-2H-pyran

https://huagongshe.com/ko/reaction/84240

반응식

참여 물질

역할이름HCID투입량
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물Ethyl AcetateHCID 8857—
반응물4-Bromo-3-fluorophenolHCID 2779153—
반응물Pyridinium.p-toluenesulfonateHCID 22033616—
용매DichloromethaneHCID 6344—
용매HeptaneHCID 8900—
생성물2-(4-bromo-3-fluorophenoxy)tetrahydro-2H-pyranHCID 5872124033%

반응 단계

Pyridinium p-toluene sulfonic acid (789 mg, 3.1 mmol) was added to a solution of 4-bromo-3-fluorophenol (4.00 g, 20.9 mmol) and 3,4-dihydro-2H-pyran (3.52 g, 41.9 mmol) in dichloromethane (105 mL, 0.2M). After 2h the reaction was quenched with saturated aqueous sodium bicarbonate and the layers were separated. The aqueous layer was extracted with dichloromethane (2×). The organic layers were combined, dried (Na2SO4), filtered and concentrated to give a colorless oil. The material was loaded onto a 25g silica guard column and run on a 330g column with 0-5% EtOAc in heptane. Desired material was concentrated down yielding 1900 mg (33%) of a clear colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846933B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-83d120aea195445e9ecc505c8ba48087
출처 메모uspto-grants-2014_09