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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1411380생성일: 2026년 10월 26일

tert-Butanol → 1,4-Bis(4-nitrophenyl)butane-1,4-dione

https://huagongshe.com/reaction/1411380

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물p-NitroacetophenoneHCID 7487—
반응물DiethylamineHCID 8021—
반응물2-Bromo-4'-nitroacetophenoneHCID 66840—
촉매ZincchlorideHCID 3007855—
용매BenzeneHCID 241—
용매WaterHCID 962—
생성물1,4-Bis(4-nitrophenyl)butane-1,4-dioneHCID 1376289161%

반응 단계

Anhydrous zinc(II)chloride (2.73 g, 20.00 mmol) was stirred in dry benzene (15 mL) while diethylamine (1.558 mL, 15.00 mmol) and t-butanol (1.435 mL, 15.00 mmol) were added, and the resulting mixture was stirred at room temperature for 90 minutes to give a cloudy solution. To this mixture was added 2-bromo-1-(4-nitrophenyl)ethanone (2.44 g, 10.00 mmol) and 1-(4-nitrophenyl)ethanone (2.477 g, 15.00 mmol), and the resulting mixture was stirred at room temperature overnight. The mixture was poured into water (50 mL) and extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over Na2SO4, filtered and concentrated. The resulting residue was triturated with dichloromethane to give an orange solid that was collected by filtration and dried to give the title compound (2.0 g, 61% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08921514B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-10a86b419e5c4031a6bbc43f13eba87d
출처 메모uspto-grants-2014_12