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HRID 576133作成日:2026年10月23日

Sodium Hydroxide → 2-(3,4-Dichloro-phenyl)-oxirane

https://huagongshe.com/ja/reaction/576133

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2-Bromo-1-(3,4-dichlorophenyl)ethanoneHCID 244751—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
生成物2-(3,4-Dichloro-phenyl)-oxiraneHCID 1352171450%

反応条件

温度0 °C

反応手順

To a solution of 2-bromo-1-(3,4-dichlorophenyl)ethanone (5.1 g, 18.96 mmol) in methanol (50 mL) at 0° C. was added sodium borohydride (2.1 g, 56.98 mmol). The reaction mixture was stirred at 0° C. for 1 hour. The pH was adjusted to 12 using 2 M sodium hydroxide solution, the solvent was then removed under reduced pressure and the residue was dissolved in dichloromethane. The resultant solution was washed with brine, dried over sodium sulfate, and concentrated under reduced pressure to give 2-(3,4-dichlorophenyl)oxirane (1.79 g, 50% crude). The crude product was used in the next step without further purification: 1H NMR (CDCl3, 500 MHz) 7.41 (d, J=8.5 Hz, 1H), 7.36 (d, J=2.0 Hz, 1H), 7.12 (dd, J=8.5, 2.0 Hz, 1H), 3.81 (dd, J=4.0, 2.5 Hz, 1H), 3.14 (dd, J=5.5, 4.0 Hz, 1H), 2.73 (dd, J=5.5, 2.5 Hz, 1H); ESI MS m/z 189 [M]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09034899B2
出典データセットuspto-grants-2015_05
ORD IDord-e055acaff45a429ebc198503ac47097a
出典メモuspto-grants-2015_05