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HRID 30633作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Triethyl phosphonoacetateHCID 13345—
反応物Sodium hydrideHCID 24758—
反応物4-(4-fluorophenyl)-4H-1,2,4-triazole-3-carbaldehydeHCID 83877613—
溶媒TetrahydrofuranHCID 8028—
生成物(2E)-3-[4-(4-fluorophenyl)-4H-1,2,4-triazol-3-yl]acrylic acidHCID 6920920877.1%

反応条件

温度0 °C

反応手順

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).

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-f587e4f7f1cf4ddc8ddbbf4804b567ee
出典メモuspto-grants-2008_09