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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393168생성일: 2026년 10월 26일

2-Bromopropane → 1-(4,6-Dimethoxy pyrimidin-5-yl)-3-methylbutan-2-ol

https://huagongshe.com/reaction/393168

반응식

참여 물질

역할이름HCID투입량
반응물2-BromopropaneHCID 6358—
반응물TetrahydrofuranHCID 8028—
반응물Ammonium ChlorideHCID 25517—
반응물4,6-Dimethoxypyrimidine-5-carbaldehydeHCID 4436645—
반응물MagnesiumHCID 5462224—
반응물HCID 178418365HCID 178418365—
생성물1-(4,6-Dimethoxy pyrimidin-5-yl)-3-methylbutan-2-olHCID 2264876054%

반응 단계

0.81 g (33 mmol) of magnesium was added to 30 ml of tetrahydrofuran, and 4.1 g (33 mmol) of 2-bromopropane was added to prepare a tetrahydrofuran solution of isopropyl magnesium bromide. 2.8 g (17 mmol) of 4,6-dimethoxypyrimidine-5-carboaldehyde was dissolved in 50 ml of tetrahydrofuran, and the solution was added to the above tetrahydrofuran solution at room temperature and reacted overnight. The reaction solution was poured into an aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was washed with an aqueous citric acid solution, water and an aqueous sodium chloride solution in this order, dried and concentrated, and the obtained oily product was purified by column chromatography (ethyl acetate:n-hexane=1:4) to obtain 1.9 g (yield: 54%) of 1-(4,6-dimethoxy pyrimidin-5-yl)-3-methylbutan-2-ol as slightly yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06806230B1
출처 데이터셋uspto-grants-2004_10
ORD IDord-d022aedc6a5e46c7be25577186f30d77
출처 메모uspto-grants-2004_10