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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
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-amine | HCID 704237 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 反応物 | Tert-butanol tetrahydrofuran | HCID 66775918 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | tert-Butanol | HCID 6386 | — |
| 生成物 | N-[4-(2,4-Dichlorophenyl)-2-thiazolyl]-2,4-dinitro-6-trifluoromethylaniline | HCID 15671712 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05298515 |
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| 出典データセット | uspto-grants-1994_03 |
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| ORD ID | ord-6295631e3f164ff297119d6e328a365f |
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| 出典メモ | uspto-grants-1994_03 |
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