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HRID 1876450作成日:2026年10月27日

Hydrochloric Acid → 5-Chloro-N1-(4'-cyanophenyl)-2,4-dinitroaniline

https://huagongshe.com/reaction/1876450

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-AminobenzonitrileHCID 13396—
反応物1,3-Dichloro-4,6-dinitrobenzeneHCID 77286—
反応物Potassium tert-butoxideHCID 23665647—
溶媒DimethylformamideHCID 6228—
生成物5-Chloro-N1-(4'-cyanophenyl)-2,4-dinitroanilineHCID 70697396—

反応手順

2,4-Dichloro-1,5-dinitrobenzene (II-1, 1.2 g, 5 mmol) and p-cyanoaniline (III-1, 0.59 g, 5 mmol) were dissolved in N,N-dimethylformamide (DFM, 10 ml). To the solution was added potassium tert-butoxide (1.4 g, 12.5 mmol) in batches in ice water bath. The mixture was allowed to react at room temperature for 45 minutes. The reaction liquid was poured into ice water. The pH value was adjusted to about 6 with dilute hydrochloric acid. The mixture was stirred for 30 minutes to precipitate a solid. The solid was filtered, washed with water to neutrality, dried, and separated on silica gel column (eluted with ethyl acetate: petroleum ether) to obtain a compound VI-1 (1.44 g, faint yellow solid). 1H NMR (CDCl3) δ ppm 7.41 (1H, s, ArH-6), 7.57 (2H, d, J=8.7 Hz, ArH-3′, 5′), 7.91 (2H, d, J=8.7 Hz, ArH-2′, 6′), 8.90 (1H, s, ArH-3), 10.07 (1H, s, NH).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08309602B2
出典データセットuspto-grants-2012_11
ORD IDord-3438de63c1f34272bac3be02e2cce82c
出典メモuspto-grants-2012_11