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HRID 415116作成日:2026年10月25日

Diisopropylethylamine → Tert-butyl 4-(3,4-dinitrophenyl)-3-methylpiperazine-1-carboxylate

https://huagongshe.com/reaction/415116

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物3,4-DinitrofluorobenzeneHCID 298675—
反応物tert-Butyl 3-methylpiperazine-1-carboxylateHCID 2756810—
溶媒DimethylacetamideHCID 31374—
生成物Tert-butyl 4-(3,4-dinitrophenyl)-3-methylpiperazine-1-carboxylateHCID 59349587—

反応条件

温度50 °C

反応手順

4-Fluoro-1,2-dinitrobenzene (0.93 g, 5.0 mmol, commercially available from Oakwood Products) and tert-butyl 3-methylpiperazine-1-carboxylate (1.0 g, 5.0 mmol) were dissolved in 3 mL of DMA, and 3 mL of diisopropylethylamine was added. The mixture was stirred at 50° C. overnight, and then cooled to room temperature, separated between ethyl acetate and water. The combined organic were washed with water, brine, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was separated by silica gel column (20% to 40% ethyl acetate in hexanes) to give 1.0 g of tert-butyl 4-(3,4-dinitrophenyl)-3-methylpiperazine-1-carboxylate. 1H-NMR (400 MHz, CDCl3): δ 8.05 (d, 2H), 6.84 (m, 2H), 3.90-4.10 (m, 3H), 3.05-3.60 (m, 4H), 1.50 (s, 9H), 1.10 (s, 3H). MS (EI): 367 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088767B2
出典データセットuspto-grants-2012_01
ORD IDord-db0ed36138b04b8ca6901f55354d3b4c
出典メモuspto-grants-2012_01