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HRID 490716作成日:2026年10月25日

Ammonium Chloride → 1-[2-(4-Bromo-phenyl)-4-isopropyl-oxazol-5-yl]-ethanol

https://huagongshe.com/reaction/490716

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物2-(4-Bromo-phenyl)4-isopropyl-oxazole-5-carbaldehydeHCID 85860626—
反応物HCID 178418573HCID 178418573—
溶媒TetrahydrofuranHCID 8028—
生成物1-[2-(4-Bromo-phenyl)-4-isopropyl-oxazol-5-yl]-ethanolHCID 5876566463%

反応手順

A solution of 2-(4-bromo-phenyl)-4-isopropyl-oxazole-5-carbaldehyde (14.4 g, 84.9 mmol) in THF (300 mL) is cooled to −78° C. and treated dropwise with methyl magnesium bromide (25 mL, 75 mmol, 3M Et2O). After 1 h, more methyl magnesium bromide (12 mL, 36 mmol) is added. The reaction mixture is stirred 1.5 h, and saturated NH4Cl solution (10 ml) is added dropwise. The mixture is partitioned between saturated NH4Cl solution (10 ml), 1N HCl (25 mL), and Et2O (300 mL). The organic layer is washed with brine (150 mL), dried (Na2SO4), and concentrated. The crude product is purified by silica gel flash chromatography using hexanes:ethyl acetate (9:1 to 5:1) to give an offwhite solid (9.5 g, 63%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07528160B2
出典データセットuspto-grants-2009_05
ORD IDord-82dfdae890274655b6ab6e259470ed3a
出典メモuspto-grants-2009_05