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HRID 839241作成日:2026年10月26日

3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carbonyl chloride → 3-(5-Nitro-2-furyl)-1-phenylpyrazole-4-carboxylic acid anhydride

https://huagongshe.com/reaction/839241

反応式

関与物質

役割名称HCID仕込み量
反応物3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carbonyl chlorideHCID 20325933—
反応物3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carboxylic acidHCID 20325964—
溶媒PyridineHCID 1049—
溶媒1,4-DioxaneHCID 31275—
生成物3-(5-Nitro-2-furyl)-1-phenylpyrazole-4-carboxylic acid anhydrideHCID 54363990—

反応手順

Add a solution of 0.64 g of 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxylic acid chloride dropwise to a warm solution of 0.60 g of 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxylic acid in 10 ml of dioxane and 0.48 ml of pyridine at 40° C. Stir the resulting reaction mixture at from 45° to 50° C for 6 hours. Draw off the formed precipitate and recrystallize it from dimethylformamide to obtain 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxylic acid anhydride [m.p. 262° to 264° C].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04093812
出典データセットuspto-grants-1978_06
ORD IDord-6cabb35fbf964e4ebfb6a7393a19d1a9
出典メモuspto-grants-1978_06