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HRID 132920作成日:2026年10月26日

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

https://huagongshe.com/reaction/132920

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 0.96 g (5.0 mmol) of 1,2-dichloro-3-nitrobenzene and 0.93 g (5.0 mmol, 1 eq) of 1-tert-butyloxycarbonylpiperazine in acetonitrile (5 mL) was added 1.38 g (10 mmol, 2 eq) of K2CO3. The mixture was heated to reflux for 48 h. The solvent was removed under reduced pressure. The crude product was partitioned between EtOAc (100 mL) and 20 mL of H2O. The organic layer was washed with H2O (2×20 mL), dried over Na2SO4 and concentrated. Column chromatography (silica, 10-20% EtOAc/hexanes) provided 1.2 g (70%) of 4-(2-chloro-6-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester. TLC (silica, 20% EtOAc/hexanes): Rf=0.45. 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), 3.56-3.38 (m, 4H), 3.10-3.00 (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-227bb913a3ec4273865c894e307e46fd
出典メモuspto-grants-2008_06