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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 402760생성일: 2026년 10월 26일

Ethyl Acetate → 1-phenyl-5-(2,4,5-trifluorophenyl)-1H-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/402760

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물TriacetoxyperiodinaneHCID 159087—
반응물Aluminium lithium hydrideHCID 21226445—
반응물ethyl 1-phenyl-5-(2,4,5-trifluorophenyl)-1H-pyrazole-4-carboxylateHCID 86685264—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물1-phenyl-5-(2,4,5-trifluorophenyl)-1H-pyrazole-4-carbaldehydeHCID 86685265—

반응 조건

온도50 °C

반응 단계

To a solution of ethyl 1-phenyl-5-(2,4,5-trifluorophenyl)-1H-pyrazole-4-carboxylate (459 mg, 1.325 mmol) in THF (5 mL) was added LAH (1.988 mL, 1.988 mmol as a 1 M THF solution) at room temperature and the reaction was then heated at 50° C. for 2 hours. The reaction was quenched with addition of 0.2 mL of water, 0.2 mL of 0.5 N NaOH and then 0.2 mL of water. The suspension was diluted with ether and was filtered through celite. Upon removal of the volatiles, the crude residue was purified by flash chromatography to afford an oil. The oil was then dissolved in 5 mL of CH2Cl2 and Dess-Martin periodinane (233.8 mg, 0.768 mmol) was added. The suspension was stirred at room temperature for 16 hours. The mixture was poured into EtOAc and was washed with brine. The organic phase was dried with Na2SO4, filtered and concentrated. The crude residue was purified by flash chromatography using a gradient of ethyl acetate/hexanes to afford the title intermediate as white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08742110B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-e874e09684ad430185186aa98612fc67
출처 메모uspto-grants-2014_06