戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 880411作成日:2026年10月26日

Diethyl Malonate → 3-(4-Nitrophenyl)propanoic acid

https://huagongshe.com/reaction/880411

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl MalonateHCID 7761—
反応物Sodium HydroxideHCID 14798—
反応物Sodium hydrideHCID 24758—
反応物4-Nitrobenzyl bromideHCID 66011—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物3-(4-Nitrophenyl)propanoic acidHCID 85526—

反応手順

Alkylation of diethyl malonate with 4-nitrobenzyl bromide using sodium hydride in THF, followed by ester hydrolysis with sodium hydroxide in water and ethanol, then heating the resulting diacid to its melting point causing decarboxylation gives 3-(4-nitro-phenyl)-propionic acid. Conversion to the acid chloride with thionyl chloride in DCM and coupling with 2-amino-4,6-dimethylpyridine affords N-(4,6-dimethyl-pyridin-2-yl)-3-(4-nitro-phenyl)-propionamide. Amide reduction with borane-dimethylsulfide in THF at reflux, methylation of the resulting amine with methyl iodide and sodium hydride in THF and finally catalytic hydrogenation over Raney nickel in methanol gives the required aniline.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08993574B2
出典データセットuspto-grants-2015_03
ORD IDord-1195b865c2c54e96bed8595ae2ea32b4
出典メモuspto-grants-2015_03