Ethyl 3-(2-fluorophenyl)-3-oxopropanoate → 2,5-bis(2-fluorophenyl)-2,4-dihydro-3H-pyrazol-3-one

HRID 241984

Reaktionsgleichung

Reaktionsgleichung von HRID 241984
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=O)[CH2:9][C:10]([O:12]CC)=O.Cl.[F:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[NH:24][NH2:25]>C(O)(=O)C>[F:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[N:24]1[C:10](=[O:12])[CH2:9][C:8]([C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[F:1])=[N:25]1

Komponenten

4

Edukt 2

HCID 296342Ethyl 3-(2-fluorophenyl)-3-oxopropanoateHCID 2723910Hydrazine, (2-fluorophenyl)-, hydrochloride (1:1)

Produkt 1

HCID 671115152,5-bis(2-fluorophenyl)-2,4-dihydro-3H-pyrazol-3-one

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Reaktionsbedingungen

Temperatur
135 °C

Versuchsvorschrift

Ethyl 3-(2-fluorophenyl)-3-oxopropanoate (2.5 g, 12 mmol) and 2-fluorophenyl hydrazine hydrochloride (1.5 g, 12 mmol, 1.0 equiv) were dissolved in acetic acid (24 mL) and placed into a preheated oil bath at 120° C. for 3 hours and then heated for an additional 2 hours at 135° C. The mixture was cooled to ambient temperature, concentrated in vacuo and then concentrated once from toluene (1×25 mL). The residue was suspended in dichloromethane, filtered and the solid was washed once with dichloromethane and dried in vacuo, providing the titled compound. The resulting filtrate was concentrated in vacuo and purified by silica gel gradient chromatography (100:0 to 65:35; hexanes:ethyl acetate), providing additional titled compound as a light brown solid.

Aufarbeitung

  1. temperatureThe mixture was cooled to ambient temperature
  2. concentrationconcentrated in vacuo
  3. concentrationconcentrated once from toluene (1×25 mL)
  4. filtrationfiltered
  5. washthe solid was washed once with dichloromethane
  6. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-b9c725f3ad864d63917729977f935ea6
Quelldatensatz
uspto-grants-2014_02
Patentnummer
US08653079B2

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