HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 595792Erstellt: 26. Oktober 2026
Ethyl Acetate → (+/-)-(3-Fluoro-4-((2,2,2-trifluoro-1-phenylethyl)carbamoyl)phenyl)boronic acid
https://huagongshe.com/reaction/595792
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | alpha-(Trifluoromethyl)benzenemethanamine | HCID 89166 | — |
| Edukt | 4-Carboxy-3-fluorophenylboronic acid | HCID 2763201 | — |
| Edukt | HCID 15569623 | HCID 15569623 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (+/-)-(3-Fluoro-4-((2,2,2-trifluoro-1-phenylethyl)carbamoyl)phenyl)boronic acid | HCID 123606597 | — |
Reaktionsschritte
A mixture of 4-borono-2-fluorobenzoic acid (54 mg, 0.294 mmol) in DCM (1468 μL) was cooled to 0° C. Then ghosez reagent N,N,3-trimethylbut-2-en-2-amine (65.8 μL, 0.587 mmol) was added and the whole mixture was stirred at rt for 20 min. The mixture was added into a mixture of TEA (246 μL, 1.762 mmol), 2,2,2-trifluoro-1-phenylethanamine (59.1 mg, 0.338 mmol) and DCM (1468 μL). The reaction was stirred at room temperature for 2 h. To the reaction mixture was added EtOAc, and washed with sat. sodium bicarbonate, water, and dried over Na2SO4. Filtered and concentrated to provide the crude product which was taken to the next step without further purification. LCMS (m/z): 342.2 (MH+), 0.84 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09242996B2 |
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| Quelldatensatz | uspto-grants-2016_01 |
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| ORD ID | ord-49a1d99c282d4e52924273ca614f866f |
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| Quellennotiz | uspto-grants-2016_01 |
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