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HRID 487912Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/487912

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzene, 2-chloro-1,5-dinitro-3-(trifluoromethyl)-HCID 67851—
Edukt4-(2,4-Dichlorophenyl)-1,3-thiazol-2-amineHCID 704237—
EduktPotassium tert-butoxideHCID 23665647—
EduktTert-butanol tetrahydrofuranHCID 66775918—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Lösungsmitteltert-ButanolHCID 6386—
ProduktN-[4-(2,4-Dichlorophenyl)-2-thiazolyl]-2,4-dinitro-6-trifluoromethylanilineHCID 1567171290%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05298515
Quelldatensatzuspto-grants-1994_03
ORD IDord-6295631e3f164ff297119d6e328a365f
Quellennotizuspto-grants-1994_03