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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 388977Erstellt: 24. Oktober 2026

Hydrochloric Acid → 1-(1H-indazol-6-yl)ethan-1-one

https://huagongshe.com/de/reaction/388977

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt1-(3-Amino-4-Methylphenyl)EthanoneHCID 342914—
EduktPotassium AcetateHCID 517044—
EduktSodium NitriteHCID 23668193—
Katalysator18-Crown-6HCID 28557—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(1H-indazol-6-yl)ethan-1-oneHCID 4411922338,6%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Concentrated HCl (2 mL) was added to a mixture of 1-(3-amino-4-methyl-phenyl)ethanone (8.4 mmol) and NaBF4 (1.2 g, 11 mmol) in H2O (10 mL) and the solution was cooled to 0° C. A solution of NaNO2 (0.58 g, 8.4 mmol) in H2O (1.5 mL) was added dropwise and the mixture was stirred at 0° C. for 30 min. The solid that formed was collected by filtration and washed with H2O (5 mL) followed by Et2O (5 mL) and dried under a reduced pressure. CH2Cl2 (20 mL), KOAc (0.91 g, 9.3 mmol) and 18-crown-6 (50 mg, 0.2 mmol) was added to the solid and the mixture was stirred at room temperature for 4 h. H2O (20 mL) was added and the layers were separated. The organic layer was dried (MgSO4) and the solvent removed at reduced pressure to afford 1-(1H-indazol-6-yl)ethanone (0.52 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08377983B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-0c91c52484e94218bfb98cd2ab0463b1
Quellennotizuspto-grants-2013_02