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HRID 30633생성일: 2026년 10월 24일

Hydrochloric Acid → (2E)-3-[4-(4-fluorophenyl)-4H-1,2,4-triazol-3-yl]acrylic acid

https://huagongshe.com/ko/reaction/30633

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Triethyl phosphonoacetateHCID 13345—
반응물Sodium hydrideHCID 24758—
반응물4-(4-fluorophenyl)-4H-1,2,4-triazole-3-carbaldehydeHCID 83877613—
용매TetrahydrofuranHCID 8028—
생성물(2E)-3-[4-(4-fluorophenyl)-4H-1,2,4-triazol-3-yl]acrylic acidHCID 6920920877.1%

반응 조건

온도0 °C

반응 단계

A mixture of 4-(4-fluorophenyl)-4H-1,2,4-triazole-3-carbaldehyde (3.83 g), ethyl diethylphosphonoacetate (5.60 g), sodium hydride (60% in oil, 0.88 g) and tetrahydrofuran (130 ml) was stirred at 0° C. for 1 hr. The reaction mixture was poured into an aqueous dilute hydrochloric acid solution and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was dissolved in a 6N aqueous hydrochloric acid solution (100 ml) and stirred for 2 hrs. with heating under reflux. Disodium hydrogen phosphate was added to neutralize the reaction mixture. The precipitated solids were collected by filtration, washed with water and dried to give (2E)-3-[4-(4-fluorophenyl)-4H-1,2,4-triazol-3-yl]acrylic acid (3.60 g, yield 76%) as pale-yellow crystals. melting point: 226-229° C. (recrystallized from ethyl acetate-hexane).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423159B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-f587e4f7f1cf4ddc8ddbbf4804b567ee
출처 메모uspto-grants-2008_09