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HRID 132912作成日:2026年10月26日

Potassium Carbonate → 1-Boc-4-(2-chloro-6-nitrophenyl)piperazine

https://huagongshe.com/reaction/132912

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2,3-DichloronitrobenzeneHCID 18555—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
溶媒AcetonitrileHCID 6342—
生成物1-Boc-4-(2-chloro-6-nitrophenyl)piperazineHCID 5876770470.2%

反応手順

To a stirred solution of 1,2-dichloro-3-nitrobenzene (0.96 g, 5.0 mmol) and piperazine-1-carboxylic acid tert-butyl ester (0.93 g, 5.0 mmol) in acetonitrile (5 mL) was added of K2CO3 (1.38 g, 10 mmol). The mixture was heated at reflux for 48 h. The solvent was removed under reduced pressure. The crude material was partitoned between EtOAc (100 mL) and H2O (20 mL). The organic layer was washed with H2O (2×20 mL), dried over Na2SO4 and concentrated. Column chromatography (silica, 10-20% EtOAc/hexanes) provided 4-(2-chloro-6-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (1.2 g, 70%). TLC (silica, 20% EtOAc/hexanes): Rf=0.45. MS (electrospray): exact mass calculated for C15H20CIN3O4, 341.1; m/z found, 364.1 [M+Na]30 . 1H NMR (400 MHz, CDCl3) 7.56 (dd, J=8.2, 1.4 Hz, 1H), 7.50 (dd, J=8.2, 1.4 Hz, 1H), 7.13 (t, J=8.2 Hz, 1H), 3.38-3.56 (m, 4H), 3.06 (m, 4H), 1.48 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07388011B2
出典データセットuspto-grants-2008_06
ORD IDord-684344737d874f748b52592cd98fb8a5
出典メモuspto-grants-2008_06