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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 595203생성일: 2026년 10월 24일

Potassium Carbonate → HCID 80107634, 화합물

https://huagongshe.com/ko/reaction/595203

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Sodium HydroxideHCID 14798—
반응물4-BromopyrazoleHCID 16375—
반응물4-(Chloromethyl)phenyl acetateHCID 148312—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
용매Ammonium ChlorideHCID 25517—
생성물HCID 80107634HCID 80107634—

반응 조건

온도40 °C

반응 단계

A mixture of 4-bromo-1H-pyrazole (500 mg, 3.40 mmol), 4-(chloromethyl)phenyl acetate (659 mg, 3.57 mmol), and potassium carbonate (1.18 g, 8.50 mmol) was diluted with DMF (5 mL) at ambient temperature. The reaction mixture was heated to 40° C. for 4 hours. The reaction mixture was then diluted with sodium hydroxide (2.0 M in water, 3.40 mL, 6.80 mmol) and stirred for an additional 30 minutes at 40° C. The reaction mixture was then cooled to ambient temperature and diluted with ethyl acetate (200 mL) and saturated aqueous ammonium chloride solution (50 mL). The organic layer was separated and washed with water (50 mL) and then brine (25 mL). The organic layer was separated, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to afford the crude product residue. The crude product residue was purified by column chromatography on silica (0-100% ethyl acetate/hexanes) to afford 4-((4-bromo-1H-pyrazol-1-yl)methyl)phenol. MS ESI calc'd. for C10H10BrN2O [M+H]+ 253 and 255. found 253 and 255. 1H NMR (500 MHz, DMSO-d6) δ 9.45 (s, 1H), 7.98 (s, 1H), 7.51 (s, 1H), 7.08 (d, J=8.5 Hz, 2H), 6.69 (dd, J=7.0 Hz, 2.0 Hz, 2H), 5.14 (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09242984B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-ff6865271c884b38a168c6098984523c
출처 메모uspto-grants-2016_01