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HRID 501219作成日:2026年10月26日

4-Nitrobenzaldehyde → 1-Methyl-4-(4-nitrobenzyl)piperazine

https://huagongshe.com/reaction/501219

反応式

関与物質

役割名称HCID仕込み量
反応物4-NitrobenzaldehydeHCID 541—
反応物1-MethylpiperazineHCID 53167—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒DichloromethaneHCID 6344—
生成物1-Methyl-4-(4-nitrobenzyl)piperazineHCID 677795—

反応手順

To a 0° C. cooled solution of 4-nitrobenzaldehyde in DCM (40 mL) was added Na(OAc)3BH (10.526 gm, 49.66 mmol) and the reacton was stirred for 10 min. To the reaction mixture was added N-methylpiperazine (9.93 g, 99.3 mmol) under nitrogen atmosphere and the reaction mixture was continued stirring at room temperature for 4 h. The progress of the reaction was monitored by TLC and upon completion of the reaction, the mixture was partitioned between DCM (20 mL) and water (15 mL) and the organic layer was separated, washed with water (2×15 mL), dried over sodium sulphate, filtered and the solvent was removed under reduced pressure to give crude residue. Washing with ether gave 1-methyl-4-(4-nitrobenzyl)piperazine (4 g). 1H NMR (CDCl3, 200 MHz) δ: 8.19 (2H, d, J=8.4 Hz), 7.53 (2H, d, J=8.4 Hz), 3.59 (2H, s), 2.47 (8H, bm), 2.29 (3H, s); m/e=236 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772245B2
出典データセットuspto-grants-2010_08
ORD IDord-f09d761aca3640698a4ac7c12f7da2a3
出典メモuspto-grants-2010_08