戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 393168作成日:2026年10月27日

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

https://huagongshe.com/reaction/393168

反応式

関与物質

役割名称HCID仕込み量
反応物2-BromopropaneHCID 6358—
反応物TetrahydrofuranHCID 8028—
反応物Ammonium ChlorideHCID 25517—
反応物4,6-Dimethoxypyrimidine-5-carbaldehydeHCID 4436645—
反応物MagnesiumHCID 5462224—
反応物HCID 178418365HCID 178418365—
生成物1-(4,6-Dimethoxy pyrimidin-5-yl)-3-methylbutan-2-olHCID 2264876054%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06806230B1
出典データセットuspto-grants-2004_10
ORD IDord-d022aedc6a5e46c7be25577186f30d77
出典メモuspto-grants-2004_10