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HRID 1429201作成日:2026年10月26日

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

https://huagongshe.com/reaction/1429201

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物p-NitroacetophenoneHCID 7487—
反応物DiethylamineHCID 8021—
反応物2-Bromo-4'-nitroacetophenoneHCID 66840—
触媒ZincchlorideHCID 3007855—
溶媒BenzeneHCID 241—
溶媒WaterHCID 962—
生成物1,4-Bis(4-nitrophenyl)butane-1,4-dioneHCID 1376289161%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08937150B2
出典データセットuspto-grants-2015_01
ORD IDord-bb7dd1484fe249dba2bb0aee9556ffbf
出典メモuspto-grants-2015_01