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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1661401Erstellt: 26. Oktober 2026

Acetone → 2-Methyl-7-(1-methylethylidene)-6,7-dihydro-8H-indeno[5,4-d][1,3]oxazol-8-one

https://huagongshe.com/reaction/1661401

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktCyanogen iodideHCID 10478—
Edukt2-Methyl-6,7-dihydro-8H-indeno[5,4-d][1,3]oxazol-8-oneHCID 57781277—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Methyl-7-(1-methylethylidene)-6,7-dihydro-8H-indeno[5,4-d][1,3]oxazol-8-oneHCID 5778127033%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

2-Methyl-6,7-dihydro-8H-indeno[5,4-d][1,3]oxazol-8-one (1.87 g, 10.0 mmol), acetone (3.68 mL, 50.0 mmol) and ICN Alumina B (manufactured by ICN, Akt.1, 20 g) were suspended in tetrahydrofuran (50 mL), and the mixture was stirred at 50° C. for 9 hr. Acetone (3.68 mL, 50.0 mmol) was added, and the mixture was further stirred for 12 hr. The reaction solution was filtered, and the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane=10/90→50/50) to give the title compound (742 mg, yield 33%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08030337B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-2dc00c06fd124a3eb56985a998ad17be
Quellennotizuspto-grants-2011_10