HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 227553Erstellt: 25. Oktober 2026
3,5-Bis(trifluoromethyl)phenylacetic acid → 2-[4-{[3,5-Bis(trifluoromethyl)phenyl]acetyl}-2-(3,4-dichlorophenyl)morpholin-2-yl]ethanol
https://huagongshe.com/reaction/227553
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 3,5-Bis(trifluoromethyl)phenylacetic acid | HCID 123587 | — |
| Edukt | 2-[2-(3,4-Dichlorophenyl)morpholin-2-YL]ethanol | HCID 15472747 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 2-[4-{[3,5-Bis(trifluoromethyl)phenyl]acetyl}-2-(3,4-dichlorophenyl)morpholin-2-yl]ethanol | HCID 18677205 | 58,6% |
Reaktionsschritte
To a solution of 3,5-bis(trifluoromethyl)phenylacetic acid (2.0 g, 7.4 mmol) in acetonitrile (20 ml), N,N′-carbonyldiimidazole (1.3 g, 8.1 mmol) was added at room temperature, then 2-[2-(3,4-dichlorophenyl)morpholin-2-yl]ethanol (2.4 g, 8.8 mmol) was further added, and the resulting mixture was stirred at room temperature for one hour. After completion of the reaction, the reaction mixture was evaporated to dryness. To the obtained residue, methylene chloride (20 ml), water (20 ml) and concentrated hydrochloric acid (2 ml) were added, and the resulting mixture was partitioned. The separated organic layer was washed successively with a 5% aqueous solution of sodium hydroxide (25 ml) and water (20 ml) and evaporated to dryness to afford the title compound [2.3 g, yield: 58.6%] as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07560549B2 |
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| Quelldatensatz | uspto-grants-2009_07 |
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| ORD ID | ord-55f01e0ef7054611848a4ecce95d2639 |
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| Quellennotiz | uspto-grants-2009_07 |
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