HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzene, 2-chloro-1,5-dinitro-3-(trifluoromethyl)- | HCID 67851 | — |
| Edukt | 4-(2,4-Dichlorophenyl)-1,3-thiazol-2-amine | HCID 704237 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Edukt | Tert-butanol tetrahydrofuran | HCID 66775918 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Produkt | N-[4-(2,4-Dichlorophenyl)-2-thiazolyl]-2,4-dinitro-6-trifluoromethylaniline | HCID 15671712 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05298515 |
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| Quelldatensatz | uspto-grants-1994_03 |
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| ORD ID | ord-6295631e3f164ff297119d6e328a365f |
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| Quellennotiz | uspto-grants-1994_03 |
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