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HRID 257849作成日:2026年10月25日

O-Xylene → 1,2-Dihydro-4-[(4-ethylaminophenyl)methyl]-5-(trifluoromethyl)-3H-pyrazol-3-one

https://huagongshe.com/reaction/257849

反応式

関与物質

役割名称HCID仕込み量
反応物O-XyleneHCID 7237—
反応物Acetamide, N-(4-(chloromethyl)phenyl)-HCID 148705—
反応物Borane;tetrahydrofuranHCID 2723981—
反応物4-[(4-acetamidophenyl)methyl]-5-(trifluoromethyl)-3H-pyrazol-3-oneHCID 19782087—
溶媒TetrahydrofuranHCID 8028—
生成物1,2-Dihydro-4-[(4-ethylaminophenyl)methyl]-5-(trifluoromethyl)-3H-pyrazol-3-oneHCID 10779467—

反応条件

温度-30 °C

反応手順

A solution of borane-THF complex (188 mL, 1M solution in tetrahydrofuran), diluted with 200 mL tetrahydrofuran, was cooled to -30° C. under N2 atmosphere. A solution of 4-[(4-acetamidophenyl)methyl]-5-(trifluoromethyl)-3H-pyrazol-3-one (6 g, prepared as in Example 1 (except that 4-acetamidobenzylchloride was reacted with the β-keto ester anion in refluxing xylene) in tetrahydrofuran (300 mL) was added over 0.75 hours and the mixture allowed to warm gradually to ambient temperature with stirring for 15 hours. The reaction mixture was refluxed for 3 hours, then cooled in ice and quenched with aqueous sodium hydroxide solution (24 mL, 2.5N). The mixture was stirred for 2 hours at ice temperature and 15 hours at room temperature. Volatile materials were removed in vacuo on the rotary evaporator. The residue was solubilized in distilled water, brought to pH 7 with dilute, aqueous HCl solution and extracted with ethyl acetate. The extracts were washed with saturated brine solution, dried over MgSO4, filtered and concentrated. The residue was dissolved in isopropyl alcohol saturated with anhydrous HCl and cooled in ice. The precipitate was collected on a suction funnel and dried under vacuum (abderhalden apparatus) to afford the title compound as a pale yellow glass; sinters at 104° C., liquefies 169°-171° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05264451
出典データセットuspto-grants-1993_11
ORD IDord-918b29f42e5a4b4b96c4a8058e47e77e
出典メモuspto-grants-1993_11