Acetone → 4-Hydroxy-3-pyridine-4-yl-4-m-tolyl-cyclopent-2-en-1-one

HRID 566719Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 566719
[N:1]1[CH:6]=[CH:5][C:4]([C:7](=O)[C:8]([C:10]2[CH:11]=[C:12]([CH3:16])[CH:13]=[CH:14][CH:15]=2)=[O:9])=[CH:3][CH:2]=1.[OH-].[K+].[CH3:20][C:21]([CH3:23])=[O:22]>>[OH:9][C:8]1([C:10]2[CH:11]=[C:12]([CH3:16])[CH:13]=[CH:14][CH:15]=2)[CH2:23][C:21](=[O:22])[CH:20]=[C:7]1[C:4]1[CH:5]=[CH:6][N:1]=[CH:2][CH:3]=1

Komponenten

4

Edukt 3

HCID 180AcetoneHCID 14797Potassium HydroxideHCID 212665371-Pyridine-4-yl-2-m-tolyl-ethane-1,2-dione

Produkt 1

HCID 212664474-Hydroxy-3-pyridine-4-yl-4-m-tolyl-cyclopent-2-en-1-one

Versuchsvorschrift

To a solution of 1-pyridine-4-yl-2-m-tolyl-ethane-1,2-dione (1.8 g, 8.0 mmole) in acetone (20 mL) was added crushed KOH (448 mg, 8.0 mmole) in one portion at r.t. The reaction mixture was stirred at that temperature for 1 hr before quenching the reaction with aqueous NH4Cl. Standard aqueous work up, followed by chromatographic purification (silica gel, hexane/ethyl acetate) gave the a mixture of the title compound and the regiosiomer, 4-hydroxy-4-pyridine-4-yl-3-m-tolyl-cyclopent-2-en-1-one. MS (m/z): Calcd. C17H15NO2(M+): 265, found (M+H)+: 265.9.

Aufarbeitung

  1. custombefore quenching
  2. customthe reaction with aqueous NH4Cl
  3. customStandard aqueous work up, followed by chromatographic purification (silica gel, hexane/ethyl acetate)
  4. customgave

Quellen und Nachweise

ORD-Eintrag
ord-44c969fb23e842dabeb9579cb11af323
Quelldatensatz
uspto-grants-2001_01
Patentnummer
US06174901B1

Notizen zur Reaktion

Wird geladen…