Water → 1H-Pyrazole-1-carboxylic acid, 4,5-dihydro-5-phenyl-, ethyl ester

HRID 1904686

Reaktionsgleichung

Reaktionsgleichung von HRID 1904686
C(N(CC)CC)C.[C:8]1([CH:14]2[NH:18][N:17]=[CH:16][CH2:15]2)[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.Cl[C:20]([O:22][CH2:23][CH3:24])=[O:21].O>C(Cl)(Cl)Cl>[CH2:23]([O:22][C:20]([N:18]1[CH:14]([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH2:15][CH:16]=[N:17]1)=[O:21])[CH3:24]

Komponenten

6

Edukt 4

HCID 962WaterHCID 8471TriethylamineHCID 10928Ethyl chloroformateHCID 1208415-Phenyl-4,5-dihydro-1H-pyrazole

Produkt 1

HCID 30790771H-Pyrazole-1-carboxylic acid, 4,5-dihydro-5-phenyl-, ethyl esterAusbeute 62 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6212ChloroformLösungsmittel

Versuchsvorschrift

Triethylamine (2.1 g) was added to a solution of 2.92 g 5-phenyl-2-pyrazoline in 50 ml chloroform, and the mixture was stirred with ice cooling. To the resulting solution, was added dropwise 2.17 g ethyl chloroformate, and the mixture was stirred for one hour. After addition of 50 ml water, the mixture was extracted with 50 ml chloroform, the extract was dried, the dried solution was concentrated, and the residue was purified by silica gel chromatography (chloroform/methanol=100/1), giving 2.7 g (yield: 62%) of pure product as oil. NMR (DMSO-d6): 1.21 (3H, t, J=6 Hz), 2.6-3.7 (2H, m), 4.18 (2H, q, J=6 Hz), 5.22 (1H, dd, J=6, 12 Hz), 6.92 (1H, t, J=2 Hz), 7.1-7.5 (5H, m).

Aufarbeitung

  1. stirringthe mixture was stirred for one hour
  2. extractionthe mixture was extracted with 50 ml chloroform
  3. customthe extract was dried
  4. concentrationthe dried solution was concentrated
  5. customthe residue was purified by silica gel chromatography (chloroform/methanol=100/1)

Quellen und Nachweise

ORD-Eintrag
ord-607f9f1440894c24a34fcae0d2c9e1f8
Quelldatensatz
uspto-grants-1989_06
Patentnummer
US04839376

Verknüpfte Notizen

Wird geladen…