戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 58146作成日:2026年10月25日

Dimethylamine → 4-[(Dimethylamino)methyl]-2-nitroaniline

https://huagongshe.com/reaction/58146

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物Sodium borohydrideHCID 4311764—
反応物4-Amino-3-nitrobenzaldehydeHCID 13237703—
触媒HCID 178460666HCID 178460666—
溶媒MethanolHCID 887—
溶媒Ethyl AcetateHCID 8857—
生成物4-[(Dimethylamino)methyl]-2-nitroanilineHCID 62183213—

反応手順

To a stirred solution of dimethylamine (4.0 mL, 2 M, 8.0 mmol) in MeOH (4 mL) was added Ti(OiPr)4 (1.15 g, 4 mmol) and the solution was stirred at room temperature for 15 minutes Then 4-amino-3-nitro-benzaldehyde (160 g, 1.0 mmol) in MeOH (2 mL) was added and the solution was stirred at room temperature overnight. Then NaBH4 (78 g, 2 mmol) was added and the solution was stirred at room temperature for 1 hour. LCMS showed major product peak. The solution was diluted with EtOAc (60 mL) and washed with water (2×100 mL) and brine (50 mL), dried over anhydrous Na2SO4. The solution was evaporated to dryness and 130 mg of crude product was collected, which was used for the next step without further purification, 1H NMR (400 MHz, DMSO-d6) δ 7.82 (s, 1H), 7.35 (br s, 2H), 7.31 (dd, 1H), 6.97 (d, 1H), 3.26 (s, 2H), 2.12 (s, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434697B2
出典データセットuspto-grants-2016_09
ORD IDord-f9d6f6fc983a4f7f931e3fb810215a6f
出典メモuspto-grants-2016_09