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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49180생성일: 2026년 10월 24일

Ethanol → 4'-Methylsulfanyl-biphenyl-2-carbaldehyde

https://huagongshe.com/ko/reaction/49180

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium CarbonateHCID 10340—
반응물2-BromobenzaldehydeHCID 81129—
반응물4-(Methylthio)phenylboronic acidHCID 2733959—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물4'-Methylsulfanyl-biphenyl-2-carbaldehydeHCID 139221796.4%

반응 단계

2-Bromobenzaldehyde (3.7 g, 20 mmol) and 4-(methylthio) benzeneboronic acid (3.36 g, 20 mmol) were dissolved in toluene (80 mL) and sodium carbonate (2M, 10 mL, 20 mmol) was added. To this reaction mixture was added ethanol (5 mL) followed by tetrakis (triphenylphosphine)palladium (240 mg, 0.2 mmol) and the reaction mixture was refluxed overnight under nitrogen atmosphere. The reaction mixture was cooled to room temperature and diluted with water (50 mL), stirred well, and the organic layer was separated. The aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with water (2×50 mL), brine (1×50 mL), dried over sodium sulfate, filtered and the filtrate concentrated under reduced pressure to give the crude product. Purification by flash column chromatography using 5% ethyl acetate in hexane gave the title compound as a colorless thick oil (4.4 g, 96% yield). 1H NMR (CDCl3) δ9.98 (s, 1H), 8.01 (dd, J=7.8 Hz and 1.2 Hz, 1H), 7.6 (dt, J=7.5 and 1.4 Hz, 2H), 7.62-7.40 (m, 2H), 7.3-7.25 (m, 3H), 2.53 (s, 3H); LRMS (APIMS) m/z 329 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706724B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-d0839809e87e4cd0b18befadcfa707df
출처 메모uspto-grants-2004_03