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HRID 1520221作成日:2026年10月25日

Dimethylformamide → ethyl 5-formyl-1-(4-methoxybenzyl)-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/1520221

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物DiisopropylamineHCID 7912—
反応物Lithium diisopropylamideHCID 2724682—
反応物ethyl 1-(4-methoxybenzyl)-1H-pyrazole-4-carboxylateHCID 44558860—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物ethyl 5-formyl-1-(4-methoxybenzyl)-1H-pyrazole-4-carboxylateHCID 8665857360.2%

反応条件

温度-78 °C

反応手順

According to Scheme 17 Step 1: Butyl lithium 2.5 M (16.9 mmol, 8.45 mL) was added to a solution of diisopropylamine (16.9 mmol, 2.37 mL) in THF (10 mL) at −78° C. and the reaction mixture was stirred at −78° C. for 5 minutes and then at room temperature. To the resulting LDA solution was added at −78° C. a solution of ethyl 1-(4-methoxybenzyl)-1H-pyrazole-4-carboxylate (7.68 mmol, 2 g) in THF (30 mL) and the reaction mixture was stirred for 5 minutes at −78° C. N,N-Dimethylformamide (61.5 mmol, 4.73 mL) was added and then the reaction mixture was stirred at room temperature. The reaction mixture was diluted with AcOEt and was washed with a saturated aqueous solution of NH4Cl. The combined organic phases were dried over MgSO4, were filtered and were evaporated. The crude mixture was purified by flash chromatography over silica gel using cyclohexane/AcOEt (100:0 to 80:20) as eluent to yield ethyl 5-formyl-1-(4-methoxybenzyl)-1H-pyrazole-4-carboxylate (4.62 mmol, 1.33 g, 60%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09073907B2
出典データセットuspto-grants-2015_07
ORD IDord-06e583d12ffe451b9a33754eabef4349
出典メモuspto-grants-2015_07