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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 900454Erstellt: 25. Oktober 2026

Dimedone → 3,6,6-trimethyl-6,7-dihydro-1H-indol-4(5H)-one

https://huagongshe.com/reaction/900454

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimedoneHCID 31358—
EduktIsonitrosoacetoneHCID 6399095—
KatalysatorZincHCID 23994—
LösungsmittelAcetic acid--water (1/1)HCID 21899381—
Produkt3,6,6-trimethyl-6,7-dihydro-1H-indol-4(5H)-oneHCID 2482079845%

Reaktionsschritte

To a solution of anti-pyruvic aldehyde-1-oxime (10 g, 1 eq) and 5,5-dimethyl-1,3-cyclohexanedione (16.1 g, 1 eq) in HOAc—H2O (7:3, 200 mL) was added zinc powder (14.95 g, 2 eq) slowly with cooling by a water bath at room temperature. The mixture then was refluxed overnight, concentrated to dryness, partitioned between brine (300 mL) and dichloromethane (300 mL). The pH was adjusted to ca. 6 with saturated aqueous NaHCO3, then the mixture was extracted with dichloromethane (3×200 mL). The organic layers were combined, dried over Na2SO4, filtered, concentrated. The crude product was purified by flash chromatography eluting with 5% ethyl acetate in dichloromethane. The combined organic fractions were concentrated, triturated in ether-hexane (2:1) for 1 hour, then filtered, washed with hexane to give the pure title compound (9 g, 45% yield) as a solid. LCMS m/z: (M+H)=178.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07358370B2
Quelldatensatzuspto-grants-2008_04
ORD IDord-67de33228f5548a4b21328879499c51d
Quellennotizuspto-grants-2008_04