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HRID 9758作成日:2026年10月24日

Hexane → 3,5-Dibromo-1-(2'-hydroxyethyl)-4-nitropyrazole

https://huagongshe.com/ja/reaction/9758

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物2-BromoethanolHCID 10898—
反応物Sodium hydrideHCID 24758—
反応物3,5-Dibromo-4-nitro-1H-pyrazoleHCID 13707994—
溶媒DimethylformamideHCID 6228—
生成物3,5-Dibromo-1-(2'-hydroxyethyl)-4-nitropyrazoleHCID 13007236—

反応条件

温度80 °C

反応手順

A solution of 3,5-dibromo-4-nitropyrazole (2) (11.0 g, 41 mmol) in DMF (52 ml) was added dropwise over 20 min to a stirred solution of NaH (1.76 g, 46 mmol; 60% dispersion in oil, prewashed with hexane under an inert atmosphere) in DMF (88 ml). After stirring for 10 minutes, a solution of 2-bromoethanol (6.4 g, 49 mmol) in DMF (14 ml) was added dropwise over 10 minutes. The reaction mixture was heated to 80° C. for 2 hours and then the DMF was evaporated off under reduced pressure. A mixture of DCM/water (100 ml, 1/1) is added to the residue and the organic phase is washed with water (50 ml). The organic phase was dried over Na2SO4 and the solvent was evaporated off under reduced pressure. The crude brown solid obtained was subsequently purified by column chromatography (5%/95% EtOAc/hexane). The yellow solid product (3.4 g) was recrystallized from a mixture of toluene/hexane (20 ml, 55%/45%) to give the 2-(3,5-dibromo-4-nitropyrazol-1-yl)ethanol (3) in the form of a white solid (2.8 g, 22%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091350B2
出典データセットuspto-grants-2006_08
ORD IDord-2a84430a84bb465c92f452a6b69a439a
出典メモuspto-grants-2006_08