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HRID 49529作成日:2026年10月24日

2-Methoxy-5-nitro-N-[[4-(trifluoromethyl)phenyl]methyl]-benzamide → 5-amino-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide

https://huagongshe.com/ja/reaction/49529

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methoxy-5-nitro-N-[[4-(trifluoromethyl)phenyl]methyl]-benzamideHCID 11057340—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒Ethyl AcetateHCID 8857—
生成物5-amino-2-methoxy-N-(4-trifluoromethylbenzyl)benzamideHCID 10903424100.6%

反応手順

To 26.6 g of 2-methoxy-5-nitro-N-(4-trifluoromethylbenzyl)benzamide were added 270 ml of ethyl acetate and 2.6 g of 10% palladium on carbon under an atmosphere of argon, then argon was replaced with hydrogen gas, and the mixture was stirred for 8 hours at room temperature under an atmosphere of hydrogen gas. Catalyst was filtered through Celite(Hyflo Super-cel) and, after washed the collected material well with ethyl acetate, the filtrate was concentrated under reduced pressure. The residue obtained was purified by means of column chromatography (silica gel, ethyl acetate) to obtain 24.5 g of 5-amino-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706763B1
出典データセットuspto-grants-2004_03
ORD IDord-25d59156999542fc86b97840bb693afb
出典メモuspto-grants-2004_03