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HRID 402760作成日:2026年10月26日

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

https://huagongshe.com/reaction/402760

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物TriacetoxyperiodinaneHCID 159087—
反応物Aluminium lithium hydrideHCID 21226445—
反応物ethyl 1-phenyl-5-(2,4,5-trifluorophenyl)-1H-pyrazole-4-carboxylateHCID 86685264—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物1-phenyl-5-(2,4,5-trifluorophenyl)-1H-pyrazole-4-carbaldehydeHCID 86685265—

反応条件

温度50 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08742110B2
出典データセットuspto-grants-2014_06
ORD IDord-e874e09684ad430185186aa98612fc67
出典メモuspto-grants-2014_06