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HRID 487912作成日:2026年10月26日

Benzene, 2-chloro-1,5-dinitro-3-(trifluoromethyl)- → N-[4-(2,4-Dichlorophenyl)-2-thiazolyl]-2,4-dinitro-6-trifluoromethylaniline

https://huagongshe.com/reaction/487912

反応式

関与物質

役割名称HCID仕込み量
反応物Benzene, 2-chloro-1,5-dinitro-3-(trifluoromethyl)-HCID 67851—
反応物4-(2,4-Dichlorophenyl)-1,3-thiazol-2-amineHCID 704237—
反応物Potassium tert-butoxideHCID 23665647—
反応物Tert-butanol tetrahydrofuranHCID 66775918—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒tert-ButanolHCID 6386—
生成物N-[4-(2,4-Dichlorophenyl)-2-thiazolyl]-2,4-dinitro-6-trifluoromethylanilineHCID 1567171290%

反応条件

温度20 °C

反応手順

A solution of 7.4 g (66 mmol) of potassium tert-butylate in 50 ml of tert-butanol was added dropwise to a vigorously stirred mixture of 8.0 g (33 mmol) of 2-amino-4-(2,4-dichlorophenyl)thiazole, 9.8 g (37 mmol) of 2,4-dinitro-6-trifluoromethylchlorobenzene and 100 ml of tetrahydrofuran/tert-butanol (1:2) at 0° to 5° C. in such a way that addition was complete after 1 hour. After a further hour at 0° C., the mixture was slowly warmed, over the course of about 2 hours, to 20° C. The mixture was then adjusted to pH 4 with glacial acetic acid and diluted with about 1 l of water. The precipitate was separated off, washed with water until neutral and dried. Yield: 90%; melting point 125° to 130° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05298515
出典データセットuspto-grants-1994_03
ORD IDord-6295631e3f164ff297119d6e328a365f
出典メモuspto-grants-1994_03