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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68608생성일: 2026년 10월 23일

Potassium Carbonate → 3-(4-Fluoro-3-(methylsulfonyl)phenyl)-4-methoxybenzaldehyde

https://huagongshe.com/ko/reaction/68608

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물5-Formyl-2-methoxyphenylboronic acidHCID 2734367—
반응물4-Bromo-1-fluoro-2-(methylsulphonyl)benzeneHCID 26985424—
촉매HCID 178418397HCID 178418397—
용매1,4-Dioxane--water (1/1)HCID 21886435—
생성물3-(4-Fluoro-3-(methylsulfonyl)phenyl)-4-methoxybenzaldehydeHCID 86681839108.1%

반응 조건

온도140 °C

반응 단계

To a solution of 5-Formyl-2-methoxyphenylboronic acid (324 mg, 1.8 mmol, 1.5 eq, Frontier Scientific, Inc., Logan, Utah, USA) in dioxane:H2O (2:1; 15 mL) was added 4-bromo-1-fluoro-2-(methylsulfonyl)benzene (300 mg, 1.2 mmol, 1.0 eq., Apollo Scientific Ltd., Stockport, Cheshire, UK), K2CO3 (496 mg, 3.6 mmol, 2 eq.) and Pd(PPh3)4 (30 mg). The mixture was stirred under nitrogen at 140° C. in a microwave for 40 min. Solvent was evaporated and the residue was dissolved in DCM and washed with water. The DCM layer was dried and evaporated. Purification via column chromatography (eluent: PE:EA=3:1) yielded 400 mg (72%) of 3-(4-fluoro-3-(methylsulfonyl)phenyl)-4-methoxybenzaldehyde (27).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822467B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-45f4597c36274a5b985838bc77ac4440
출처 메모uspto-grants-2014_09