돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1021216생성일: 2026년 10월 26일

1,4-Dioxane → 2-(4-morpholinyl)-5-Pyrimidinol

https://huagongshe.com/reaction/1021216

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DioxaneHCID 31275—
반응물Potassium AcetateHCID 517044—
반응물Bis(pinacolato)diboraneHCID 2733548—
반응물4-(5-Bromopyrimidin-2-yl)morpholineHCID 5144362—
촉매HCID 178418476HCID 178418476—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2-(4-morpholinyl)-5-PyrimidinolHCID 1987103541.1%

반응 조건

온도80 °C

반응 단계

A mixture of 4-(5-bromopyrimidin-2-yl)morpholine (2 g), 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi-1,3,2-dioxaborolane (2.5 g), bis(triphenylphosphine)palladium chloride (180 mg), potassium acetate (2.5 g), and dioxane (20 ml) was stirred at 80° C. overnight under argon atmosphere. Water and EtOAc were added to the reaction mixture, and the organic layer was dried over MgSO4 and concentrated under reduced pressure. The obtained residue was mixed with THF (10 ml) and water (10 ml), and sodium perborate.tetrahydrate (3.5 g) was added thereto, followed by stirring at room temperature overnight. Then, a saturated aqueous ammonium chloride solution was added thereto. The aqueous layer was extracted with EtOAc, and the organic layer was dried over MgSO4 and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/EtOAc) to obtain 2-(morpholin-4-yl)pyrimidin-5-ol (610 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08716470B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-0113e6ff68014374a71b35e65f9ae46c
출처 메모uspto-grants-2014_05