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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 355684생성일: 2026년 10월 24일

1-Chloro-2,6-dinitrobenzene → 2-((2,6-Dinitrophenyl)amino)benzyl alcohol

https://huagongshe.com/ko/reaction/355684

반응식

참여 물질

역할이름HCID투입량
반응물1-Chloro-2,6-dinitrobenzeneHCID 11814—
반응물2-Aminobenzyl alcoholHCID 21439—
용매TriethylamineHCID 8471—
생성물2-((2,6-Dinitrophenyl)amino)benzyl alcoholHCID 5408861854.3%

반응 단계

2.85 g (14 mmol) of 1-chloro-2,6-dinitrobenzene and 1.73 g (14 mmol) of 2-aminobenzyl alcohol were dissolved in 30 ml of triethylamine and heated under reflux for 24 hours. After concentrating, the residue was purified by silica gel column chromatography. Thus 2.2 g of 2-((2,6-dinitrophenyl)amino) benzyl alcohol was obtained. 0.29 g (1 mmol) of this powder was dissolved in 20 ml of dry dimethylformamide. After adding 40 mg (1 mmol) of sodium hydride (in oil, content: 60%), the reaction mixture was stirred at room temperature for 15 minutes and then at 150° C. for 2 hours. After cooling, 200 ml of ethyl acetate was added thereto and the mixture was washed with water, dried over magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography. Thus 0.14 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-d1d738ecaef74f598e25d94a76ef322b
출처 메모uspto-grants-1998_11