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HRID 17060作成日:2026年10月25日

Sodium Hydroxide → 3-Bromo-5-(trifluoromethyl)benzaldehyde

https://huagongshe.com/reaction/17060

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物TriacetoxyperiodinaneHCID 159087—
反応物[3-Bromo-5-(trifluoromethyl)phenyl]methanolHCID 29919767—
溶媒DichloromethaneHCID 6344—
生成物3-Bromo-5-(trifluoromethyl)benzaldehydeHCID 16115438—

反応条件

温度0 °C

反応手順

A solution of [3-bromo-5-(trifluoromethyl)phenyl]methanol (409 mg, 1.61 mmol) in CH2Cl2 (25 mL) was cooled to 0° C. and then Dess-Martin periodinane (1.02 g, 2.41 mmol) was added. The reaction was stirred at 0° C. for 30 minutes and then warmed to room temperature. After stirring at room temperature for thirty minutes, the reaction was poured into 1N NaOH (25 mL). The mixture was extracted with EtOAc (100 mL), and the organic extracts were washed with 1N NaOH (25 mL), then brine (25 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 25% EtOAc/hexanes afforded 3-bromo-5-(trifluoromethyl)benzaldehyde. Rf=0.60 (25% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 10.02 (s, 1H), 8.20 (s, 1H), 8.07 (s, 1H), 8.02 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737295B2
出典データセットuspto-grants-2010_06
ORD IDord-74f4dd60082d45da8113fa788f74dd72
出典メモuspto-grants-2010_06