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Dimethylformamide → ethyl (+/-)-4-formyl-alpha-phenyl-1H-pyrazole-l-acetate

HRID 1756948
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1756948
P(Cl)(Cl)(Cl)=O.[C:6]1([CH:12]([N:18]2[CH:22]=[CH:21][CH:20]=[N:19]2)[C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.CN([CH:26]=[O:27])C>>[CH:26]([C:21]1[CH:20]=[N:19][N:18]([CH:12]([C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=2)[C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:22]=1)=[O:27]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 6228Dimethylformamide2×HCID 24813Phosphorus oxychlorideHCID 4257156ethyl 2-phenyl-2-(1H-pyrazol-1-yl)acetate

Produkt 1

HCID 10563150ethyl (+/-)-4-formyl-alpha-phenyl-1H-pyrazole-l-acetateAusbeute 89 %

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

Phosphorous oxychloride (7.0 mL, 75 mmol) was added dropwise to 14 mL DMF at 0° C. under an atmosphere of N2. The resulting solution was stirred for 0.5 hour and then a solution of ethyl (±)-α-phenyl-1H-pyrazole-1-acetate (5.76 g, 25 mmol) in 5 mL DMF was added dropwise. The resulting orange solution was warmed to 70° C. for 16 hours. The reaction mixture was cooled to 0° C. and carefully quenched with saturated Na2CO3 solution. The reaction mixture was partitioned between water and ether and the ether layer was dried over MgSO4, filtered, and concentrated to give an orange oil. Chromatography (15% EtOAc/hexanes on silica) gave 5.73 g (89%) of the title compound as a yellow/green oil which solidified upon standing; mp 68°-70° C.

Aufarbeitung

  1. temperatureThe reaction mixture was cooled to 0° C.
  2. customcarefully quenched with saturated Na2CO3 solution
  3. customThe reaction mixture was partitioned between water and ether
  4. dry with materialthe ether layer was dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto give an orange oil

Quellen und Nachweise

ORD-Eintrag
ord-7f9ba16a1aa146df8fffca99d24b9428
Quelldatensatz
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05441975

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