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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 576133생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/576133

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참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물2-Bromo-1-(3,4-dichlorophenyl)ethanoneHCID 244751—
반응물Sodium borohydrideHCID 4311764—
용매MethanolHCID 887—
생성물2-(3,4-Dichloro-phenyl)-oxiraneHCID 1352171450%

반응 조건

온도0 °C

반응 단계

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]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09034899B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-e055acaff45a429ebc198503ac47097a
출처 메모uspto-grants-2015_05