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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 56545생성일: 2026년 10월 24일

Potassium Hydroxide → 5-Bromo-2-(difluoromethoxy)-1,3-dimethoxybenzene

https://huagongshe.com/ko/reaction/56545

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물Bromodifluoromethyl diethylphosphonateHCID 144101—
반응물4-Bromo-2,6-dimethoxyphenolHCID 14845876—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물5-Bromo-2-(difluoromethoxy)-1,3-dimethoxybenzeneHCID 5843207162%

반응 조건

온도-78 °C

반응 단계

5-Bromo-2-(difluoromethoxy)-1,3-dimethoxybenzene was synthesized from 4-bromo-2,6-dimethoxyphenol according to the procedure of Zafrani, Y. Tetrahedron 2009, 65, 5278 as follows. To a solution of 4-bromo-2,6-dimethoxyphenol (1.08 g, 4.6 mmol) in MeCN (27 mL) was added a solution of KOH (5.0 g, 89 mmol) in H2O (27 mL). The mixture was immediately cooled over a −78° C. bath and diethyl(bromodifluoromethyl)phosphonate (1.6 mL, 8.9 mmol) was added. The flask was sealed with a septum and the cold bath was removed. The mixture was stirred for a total of 3.5 hrs during which time the septum was ejected from the flask. The reaction was diluted with EtOAc and the layers were separated. The aqueous layer was extracted with EtOAc and the combined organics were washed with 1 M NaOH, H2O and brine then dried over Na2SO4 and concentrated in vacuo. Purification by chromatography (0-30% EtOAc-hexanes) provided 5-bromo-2-(difluoromethoxy)-1,3-dimethoxybenzene as a white solid (0.808 g, 62% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434707B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-11df3402760d45b2a0c38bdeab5e3b2c
출처 메모uspto-grants-2016_09