돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 355683생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/355683

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물1-Chloro-2,6-dinitrobenzeneHCID 11814—
반응물DiisopropylethylamineHCID 81531—
반응물4-Aminobenzene-1,3-diol hydrochlorideHCID 13408822—
용매DimethylformamideHCID 6228—
생성물4-((2,6-Dinitrophenyl)amino)resorcinolHCID 5406325479.6%

반응 단계

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-diisopropylethyl-amine 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05834462
출처 데이터셋uspto-grants-1998_11
ORD IDord-11d116a1b02e44bbad7779b9446031ff
출처 메모uspto-grants-1998_11