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HRID 30674作成日:2026年10月25日

Malonic Acid → (2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylic acid

https://huagongshe.com/reaction/30674

反応式

関与物質

役割名称HCID仕込み量
反応物Malonic AcidHCID 867—
反応物PiperidineHCID 8082—
反応物Sodium HydroxideHCID 14798—
反応物5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehydeHCID 23157484—
溶媒TolueneHCID 1140—
溶媒DiglymeHCID 8150—
生成物(2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylic acidHCID 6920898190%

反応条件

温度92.5 °C

反応手順

To a mixture of 5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehyde (3.00 g), malonic acid (1.99 g) and bis(2-methoxyethyl) ether (9 mL) was added dropwise piperidine (1.89 mL) over about 10 min. The mixture was stirred at 90-95° C. for 1 hr. and further at 105-110° C. for 4 hrs. After cooling to 25° C., toluene (12 mL) and 1N aqueous sodium hydroxide solution (15 mL) were added and the mixture was stirred. The aqueous layer was separated and the organic layer was extracted with 1N aqueous sodium hydroxide solution (6 mL). The aqueous layers were combined and washed with toluene. The layers were adjusted to pH 3.5-4.0 with 2N hydrochloric acid at 20-30° C. and water (9 mL) was added dropwise. After stirring at 25° C. for 1 hr., the precipitated crystals were collected by filtration and washed with 20% ethanol to give (2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylic acid (3.24 g, yield 90%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423159B2
出典データセットuspto-grants-2008_09
ORD IDord-db6aa61893614edf9ca87b9570f1139c
出典メモuspto-grants-2008_09