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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1269822Erstellt: 25. Oktober 2026

Acetic Anhydride → 1-acetyl-6-methyl-1H-indazol-5-yl acetate

https://huagongshe.com/reaction/1269822

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktIsoamyl NitriteHCID 8053—
EduktPotassium AcetateHCID 517044—
Edukt4-(Acetylamino)-2,5-dimethylphenyl acetateHCID 19078613—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-acetyl-6-methyl-1H-indazol-5-yl acetateHCID 6943075846%

Reaktionsschritte

Acetic anhydride (0.96 ml, 10.2 mmol), tetrabutylammonium bromide (55 mg, 0.169 mmol), potassium acetate (665 mg, 6.78 mmol) and isoamyl nitrite (0.592 ml, 4.41 mmol) were added to a solution of 4-(acetylamino)-2,5-dimethylphenyl acetate (750 mg, 3.39 mmol) in ethyl acetate (7.5 ml) at room temperature, and the resulting mixture was refluxed. After 9 hours, the reaction solution was poured into water (50 ml) and extracted with ethyl acetate (50 ml×2), and the organic layer was dried over anhydrous magnesium sulfate. The organic layer dried was concentrated under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent: hexane/ethyl acetate) to obtain 1-acetyl-6-methyl-1H-indazol-5-yl acetate (359 mg, 46%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07199147B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-3617566acb644d40b8982d67857f84d5
Quellennotizuspto-grants-2007_04