戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 371690作成日:2026年10月26日

Ethanol → Benzenamine, N-methoxy-2,6-dinitro-4-(trifluoromethyl)-

https://huagongshe.com/reaction/371690

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物TriethylamineHCID 8471—
反応物4-Chloro-3,5-dinitrobenzotrifluorideHCID 9809—
反応物O-Methylhydroxylamine hydrochlorideHCID 521874—
溶媒Ethyl AcetateHCID 8857—
生成物Benzenamine, N-methoxy-2,6-dinitro-4-(trifluoromethyl)-HCID 12102672—

反応手順

To a solution prepared from 27.0 g. (0.1 mole) of 4-chloro-3,5-dinitrobenzotrifluoride in 200 ml. of ethanol there was added 25.25 g. (0.25 mole) of triethylamine, and 12.5 g. (0.15 mole) of methoxyamine hydrochloride. Upon the addition of the methoxyamine hydrochloride, the temperature of the reaction mixture rose to about 50° C. The reaction mixture was allowed to stir for about 11/2 hours and the reaction product mixture was worked up by diluting with ethyl acetate, washing several times with dilute hydrochloric acid and water, and drying the organic layer over anhydrous magnesium sulfate. The drying agent was filtered off and the filtrate concentrated on the steam bath to leave a residue. The residue was allowed to chill over the weekend in the refrigerator and crystals separated. The crystalline product was filtered off. It had a melting point of about 135°-137° C., weighed 21.0 g., and was identified by NMR spectrum and elemental analyses as 2,6-dinitro-N-methoxy-α,α,α-trifluoro-p-toluidine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04087460
出典データセットuspto-grants-1978_05
ORD IDord-751c3818556047f8824abb978828dfb8
出典メモuspto-grants-1978_05