HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 341736Erstellt: 26. Oktober 2026
Water → Benzene, 1-bromo-3-fluoro-4-(methylthio)-2-(trifluoromethyl)-
https://huagongshe.com/reaction/341736
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Dimethyl Disulfide | HCID 12232 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Edukt | 4-Bromo-2-fluoro-3-(trifluoromethyl)aniline | HCID 53669714 | — |
| Katalysator | Copper | HCID 23978 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Sulfuric Acid | HCID 1118 | — |
| Produkt | Benzene, 1-bromo-3-fluoro-4-(methylthio)-2-(trifluoromethyl)- | HCID 53772445 | — |
Reaktionsschritte
A solution of sodium nitrite (11.2 g) in concentrated sulphuric acid was added to a stirred cooled suspension of 4-bromo-2-fluoro-3-trifluoromethylaniline (40 g) in glacial acetic acid while maintaining the temperature below 5° C. The mixture was stirred at 5° C. for one and a half hours. The resultant mixture was added gradually to a mixture of dimethyl disulphide (20 ml) and copper power (0.224 g) in glacial acetic acid at 45° C. It was stirred and heated at 70° C. for 3 hours. It was cooled, poured into water, extracted with ether, washed with water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness and purified by column chromatography eluted with petroleum spirit (b.p. 60°-80° C.) to give 6-bromo-2-fluoro-3-(methylsulphenyl)benzotrifluoride (30.6 g) as an orange oil NMR (CDCl3) 2.45(s,3H), 7.25(t,1H), 7.5(d,1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05856274 |
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| Quelldatensatz | uspto-grants-1999_01 |
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| ORD ID | ord-53ab50e7bcd246aa8df902be426b2b2b |
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| Quellennotiz | uspto-grants-1999_01 |
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