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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1178539생성일: 2026년 10월 26일

Water → 4-Chloro-2-(3-dimethylaminomethyl-2-methylsulfanyl-phenoxy)-benzonitrile

https://huagongshe.com/reaction/1178539

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Cesium carbonateHCID 10796—
반응물4-Chloro-2-fluorobenzonitrileHCID 93655—
반응물3-Dimethylaminomethyl-2-methylsulfanyl-phenol hydrobromideHCID 21930351—
용매DimethylformamideHCID 6228—
생성물4-Chloro-2-(3-dimethylaminomethyl-2-methylsulfanyl-phenoxy)-benzonitrileHCID 990216158%

반응 단계

4-Chloro-2-fluorobenzonitrile (0.974 g, 6.26 mmol), 3-dimethylaminomethyl-2-methylsulfanyl-phenol hydrobromide (1.74 g, 6.26 mmol) and cesium carbonate (4.08 g, 12.5 mmol) were heated with stirring in dry DMF (4 mL) at 50° C. for 17 h. The reaction was complete by LC/MS analysis. The reaction mixture was cooled, poured into water and extracted with ethyl acetate. The ethyl acetate layer was separated, washed with water (1×), 10% sodium carbonate solution (2×), water (2×), brine (1×), and dried over MgSO4. After filtration, the solvent was removed in vacuo to yield 4-chloro-2-(3-dimethylaminomethyl-2-methylsulfanyl-phenoxy)-benzonitrile (1.2 g, 58%) as a yellow oil. Fumaric acid (92 mg, 0.3 mmol) in methanol (5 mL) was added to 4-chloro-2-(3-dimethylaminomethyl-2-ethylsulfanyl-phenoxy)-benzonitrile (91 mg, 0.26 mmol). The solvent was removed in vacuo and diethyl ether (20 mL) was added with stirring. After 17 h, 4-chloro-2-(3-dimethylaminomethyl-2-methysulfanyl-phenoxy)-benzonitrile fumarate (63.2 mg, 47%) was filtered off as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07276528B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-51f58a80ca9f4c7691a6ff1806238f8e
출처 메모uspto-grants-2007_10