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HRID 1170847Erstellt: 26. Oktober 2026

2-[(Dimethylamino)methylidene]cyclohexane-1,3-dione → 1-(3,4-dichlorophenyl)-1,5,6,7-tetrahydro-4H-indazol-4-one

https://huagongshe.com/reaction/1170847

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-[(Dimethylamino)methylidene]cyclohexane-1,3-dioneHCID 359353—
EduktSodium AcetateHCID 517045—
Edukt(3,4-Dichlorophenyl)hydrazine monohydrochlorideHCID 3084323—
LösungsmittelAcetic AcidHCID 176—
Lösungsmittel1-ButanolHCID 263—
Produkt1-(3,4-dichlorophenyl)-1,5,6,7-tetrahydro-4H-indazol-4-oneHCID 2311290456%

Reaktionsschritte

A mixture of 1-(3,4-dichlorophenyl)hydrazine hydrochloride (6.78 g, 31.8 mmol) and anhydrous sodium acetate (2.60 g, 31.8 mmol) in n-BuOH (20 mL) is slowly added to a solution of 2-((dimethylamino)methylene)cyclohexane-1,3-dione (5.32 g, 31.8 mmol) in n-BuOH (100 mL) and acetic acid (5 mL). The resulting mixture is heated to reflux during 2 hours, effecting follow-up of the reaction by TLC. The solvent is evaporated at reduced pressure, the residue is diluted in AcOEt and washed with H2O. The solvent is next evaporated, and the crude is purified by silica-gel chromatography, to obtain 1-(3,4-dichlorophenyl)-1,5,6,7-tetrahydro-4H-indazol-4-one (5.0 g, 17.79 mmol, 56%, orange solid). 1H RMN (300 MHz, CDCl3): δ 2.17 (m, 2H), 2.51 (m, 2H), 2.96 (t, J=6.1 Hz, 2H), 7.36 (t, J=8.6 Hz, J′=2.4 Hz, 1H), 7.54 (d, J=8.6 Hz, 1H), 7.64 (d, J=2.4 Hz, 1H), 8.02 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07829559B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-d29e30af4694488f895c26e173c2e7d1
Quellennotizuspto-grants-2010_11