P-Cresol → 4-Methylphenyl 2,4,5-trifluorobenzoate
Reaktionsgleichung
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[F:9][C:10]1[CH:18]=[C:17]([F:19])[C:16]([F:20])=[CH:15][C:11]=1[C:12](O)=[O:13].CCCCCCC>CCOC(C)=O>[F:9][C:10]1[CH:18]=[C:17]([F:19])[C:16]([F:20])=[CH:15][C:11]=1[C:12]([O:8][C:5]1[CH:6]=[CH:7][C:2]([CH3:1])=[CH:3][CH:4]=1)=[O:13]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 40 °C
Versuchsvorschrift
The title compound can also be prepared according to the following method: 4-methylphenol (80.0 g, 739.8 mmol) was added to a suspension of 2,4,5-trifluorobenzoic acid (136.8 g, 776.8 mmol) and 1,1-carbonyldiimidazole (83-85% wt, 163.6 g, 849.7 mmol) in EtOAc (1.20 L) at 40° C. The reaction mixture was stirred at 40° C. for 2 hours, then cooled to 20° C. and washed with water (480 mL), a 0.5 M aqueous solution of sodium hydroxide (2×400 mL) and water (400 mL). The organics were concentrated in vacuo and azeotroped with heptane to give a yellow oil. Heptane (640 mL) was added and the reaction was stirred at room temperature for 16 hours. A seed was used to facilitate the formation of a suspension. The resulting suspension was cooled to 10° C. and filtered. The residue was washed with cold heptane (80 mL) and dried to afford the title compound as an off white solid (147.5 g, 75%):
Aufarbeitung
- customat 40° C
- temperaturecooled to 20° C.
- washwashed with water (480 mL)
- concentrationThe organics were concentrated in vacuo
- customazeotroped with heptane
- customto give a yellow oil
- stirringthe reaction was stirred at room temperature for 16 hours
- temperatureThe resulting suspension was cooled to 10° C.
- filtrationfiltered
- washThe residue was washed with cold heptane (80 mL)
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-bbbcfe5b38ea45d39bf5dfe637a41a05
- Quelldatensatz
- uspto-grants-2013_11
- Patentnummer
- US08592629B2
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