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HRID 15064作成日:2026年10月24日

Tetrahydrofuran → 2-Chloro-4-(4-fluorobenzyloxy)pyrimidine

https://huagongshe.com/ja/reaction/15064

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物4-Fluorobenzylic alcoholHCID 68022—
反応物2,4-DichloropyrimidineHCID 77531—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
生成物2-Chloro-4-(4-fluorobenzyloxy)pyrimidineHCID 8607073068%

反応手順

n-Butyl lithium (2.6 M n-hexane solution, 10.1 mL) was added to tetrahydrofuran solution (12 mL) of 4-fluorobenzyl alcohol (3.08 mL) at −78° C., and stirred at the same temperature for 30 minutes. This reaction liquid was gradually added to tetrahydrofuran suspension (24 mL) of 2,4-dichloropyrimidine (4.0 g) and stirred at room temperature for 2 hours. After addition of water, the reaction liquid was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. Concentrating the solvent under reduced pressure, the residue was crystallized from mixed solvent of chloroform and hexane to provide the title compound (4.36 g, 68%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732456B2
出典データセットuspto-grants-2010_06
ORD IDord-ab4bf3d2c4494cc991525056ab6da85b
出典メモuspto-grants-2010_06