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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30674생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/30674

반응식

참여 물질

역할이름HCID투입량
반응물Malonic AcidHCID 867—
반응물PiperidineHCID 8082—
반응물Sodium HydroxideHCID 14798—
반응물5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehydeHCID 23157484—
용매TolueneHCID 1140—
용매DiglymeHCID 8150—
생성물(2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylic acidHCID 6920898190%

반응 조건

온도92.5 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423159B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-db6aa61893614edf9ca87b9570f1139c
출처 메모uspto-grants-2008_09