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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40698생성일: 2026년 10월 23일

Hydrochloric Acid → 2-(4-Bromophenoxy)pyridine

https://huagongshe.com/ko/reaction/40698

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-BromophenolHCID 7808—
반응물2-FluoropyridineHCID 9746—
반응물Sodium hydrideHCID 24758—
용매DimethylformamideHCID 6228—
생성물2-(4-Bromophenoxy)pyridineHCID 2320193577.2%

반응 단계

4-Bromophenol (2 g, 11.5 mmol) is placed in 10 ml of anhydrous DMF under nitrogen. Sodium hydride (0.51 g, 127 mmol) is added. After stirring for 20 min at ambient temperature, 2-fluoropyridine (1.05 ml, 12.1 mmol) is added and the reaction medium is heated at 105° C. for 7 h. After hydrolysis, the pH is adjusted to 8 with a 1N aqueous solution of HCl. The reaction medium is then extracted with ethyl acetate. The organic phase is washed with a saturated aqueous sodium chloride solution, dried over MgSO4 and concentrated to dryness. The crude product obtained is chromatographed on silica gel, elution being carried out with a gradient of ethyl acetate in heptane ranging from 0% to 30%. 2.22 g of expected 2-(4-bromo-phenoxy)pyridine are obtained,

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530477B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-55b4b911dcaf480b88a1b9de8397e19c
출처 메모uspto-grants-2013_09