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HRID 1456935作成日:2026年10月26日

Tetrahydrofuran → 4-((2,6-Dinitrophenyl)amino)resorcinol

https://huagongshe.com/reaction/1456935

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物1-Chloro-2,6-dinitrobenzeneHCID 11814—
反応物DiisopropylethylamineHCID 81531—
反応物4-Aminobenzene-1,3-diol hydrochlorideHCID 13408822—
溶媒DimethylformamideHCID 6228—
生成物4-((2,6-Dinitrophenyl)amino)resorcinolHCID 5406325479.6%

反応手順

6 g (30 mmol) of 1-chloro-2,6-dinitrobenzene and 4.8 g (30 mmol) of 4-aminoresorcinol hydrochloride were added to 300 ml of a mixture of tetrahydrofuran with dimethylformamide (1:1). After adding 7.8 g (60 mmol) of N,N-diisopropylethylamine thereto, the obtained mixture was stirred at room temperature for 24 hours. Then the solvent was distilled off under reduced pressure and the residue was dissolved in ethyl acetate and washed with a saturated aqueous solution of sodium chloride. Then it was dried over magnesium sulfate and concentrated and the residue was purified by silica gel column chromatography. Thus 6.95 g of 4-[(2,6-dinitrophenyl)amino]resorcinol was obtained. This product was dissolved in 125 ml of dimethylformamide and 25 ml of N,N-diisopropylethylamine was added thereto. After heating at 100° C. for 2 hours, the reaction mixture was concentrated and the residue was dissolved in ethyl acetate, washed with water, dried over magnesium sulfate and concentrated to dryness. Thus 5.4 g of the title compound was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05846969
出典データセットuspto-grants-1998_12
ORD IDord-98a255e7e460486b95536713285ef828
出典メモuspto-grants-1998_12