HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 445114Erstellt: 24. Oktober 2026
Hydrochloric Acid → [4-[2-Chloro-4-(trifluoromethyl)phenoxy]phenyl]boronic acid
https://huagongshe.com/de/reaction/445114
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Benzene, 2-chloro-1-fluoro-4-(trifluoromethyl)- | HCID 157153 | — |
| Edukt | 4-Hydroxyphenylboronic acid | HCID 2734360 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Produkt | [4-[2-Chloro-4-(trifluoromethyl)phenoxy]phenyl]boronic acid | HCID 67972395 | 13,2% |
Reaktionsschritte
A solution of 2-chloro-1-fluoro-4-(trifluoromethyl)benzene (0.95 g), (4-hydroxyphenyl)boronic acid (0.66 g), and potassium carbonate (1.65 g) in DMSO (5.0 mL) was heated with stirring at 130° C. for 20 hours. The resultant reaction mixture was left to be cooled down and was poured into an ice water, and pH of the resultant reaction mixture was adjusted to around 2 with a 10% hydrochloric acid, followed by extracting the reaction mixture with ethyl acetate. From the organic phase, the solvent was distilled off under reduced pressure, and the resultant residue was purified by silica gel column chromatography (eluate; n-hexane:ethyl acetate 100:0 to 50:50) to obtain the subject compound (0.20 g) as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08476287B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-41a8d61ec7344509a0cbc969aa69eb85 |
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| Quellennotiz | uspto-grants-2013_07 |
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