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HRID 1835629생성일: 2026년 10월 23일

2,5-Dimethyl-p-phenylenediamine → (4-Amino-2,5-dimethyl-phenylamino)-2,6-di-tert-butyl-phenol

https://huagongshe.com/ko/reaction/1835629

반응식

참여 물질

역할이름HCID투입량
반응물2,5-Dimethyl-p-phenylenediamineHCID 160824—
반응물Phenol, 4-(bromomethyl)-2,6-bis(1,1-dimethylethyl)-HCID 612973—
용매TetrahydrofuranHCID 8028—
생성물(4-Amino-2,5-dimethyl-phenylamino)-2,6-di-tert-butyl-phenolHCID 86759498—

반응 단계

4-Bromomethyl-2,6-di-tert-butyl-phenol (2.42 g, 0.008 mole) was dissolved in 50 mL of dry tetrahydrofuran. In a separate conical flask 2,5-dimethyl-benzene-1,4-diamine (2.17 g, 0.016 mole) was dissolved in 25 mL of tetrahydrofuran and solution was transferred to a cylindrical funnel with pressure equalizing tube. Three-necked round-bottom flask containing solution of 4-Bromomethyl-2,6-di-tert-butyl-phenol was kept in oil-bath at 85° C. Solution in the flask was continuously stirred with the help of magnetic stirrer. 2,5-dimethyl-para-phenylene diamine solution was added drop-by-drop, from funnel to the flask in acidic medium for a span of 4-5 hours till all the solution was poured out. The reaction was terminated after that and the final reaction mixture was allowed to attain room temperature. Product was separated by solvent evaporation. The product was purified using silica gel column chromatography. Product was identified by 1H-NMR. The yield of 4-[(4-Amino-2,5-dimethyl-phenylamino)-2,6di-tert-butyl-phenol is 1.86 g (65%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06770785B1
출처 데이터셋uspto-grants-2004_08
ORD IDord-86f04b26e8e04787a808175bb016cfe7
출처 메모uspto-grants-2004_08