HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 266554Erstellt: 23. Oktober 2026
Carbon Dioxide → Benzoic acid, 2-(methylthio)-4-(trifluoromethyl)-
https://huagongshe.com/de/reaction/266554
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Benzene, 1-bromo-2-(methylthio)-4-(trifluoromethyl)- | HCID 11000144 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Benzoic acid, 2-(methylthio)-4-(trifluoromethyl)- | HCID 11085762 | — |
Reaktionsschritte
n-Butyllithium (2.5M solution in hexane; 25 ml) was added under an inert atmosphere to a stirred solution 4-bromo-3-methylsulphenylbenzotrifluoride (16.4 g) in ether whilst maintaining the temperature below -70° C. The mixture was stirred at -70° C. for 2 hours and then poured onto solid carbon dioxide pellets. The mixture was stirred for 10 minutes and aqueous hydrochloric acid was added. The layers were separated and the aqueous layer was extracted with ether. The combined organic layers were washed with water, dried (anhydrous magnesium sulphate) and filtered. The filtrate was evaporated and the residue was triturated with cyclohexane and filtered to give 2-methylsulphenyl-4-trifluoromethylbenzoic acid (12.4 g) as a white solid, NMR [CDCl3 +DMSO-d6 ]: 2.45 (s,3H), 7.2(d, 1H), 7.3(s, 1H), 8.0 (d, 1H), 10.7-11.1 (bs, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05650533 |
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| Quelldatensatz | uspto-grants-1997_07 |
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| ORD ID | ord-a6fbdd378e2747e8954f2dd49973b3d8 |
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| Quellennotiz | uspto-grants-1997_07 |
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