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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1827911Erstellt: 26. Oktober 2026

N-Methylmorpholine N-oxide monohydrate → 2-Hydroxy-6-methoxy-3,3-dimethyl-2,3-dihydro-1H-benzo[b]pyrano[3,2-h]-acridine-1,7(14H)-dione

https://huagongshe.com/reaction/1827911

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Methylmorpholine N-oxide monohydrateHCID 2724197—
Edukt6-Methoxy-3,3-dimethyl-3,14-dihydro-7H-benzo[b]pyrano[3,2-h]acridin-7-oneHCID 22064514—
EduktSodium BisulfiteHCID 23665763—
KatalysatorOsmium TetroxideHCID 30318—
Lösungsmitteltert-ButanolHCID 6386—
Lösungsmittelt-Butanol tetrahydrofuran waterHCID 22124471—
Produkt2-Hydroxy-6-methoxy-3,3-dimethyl-2,3-dihydro-1H-benzo[b]pyrano[3,2-h]-acridine-1,7(14H)-dioneHCID 22064508—

Reaktionsschritte

To a solution of 1.33 mmol of the compound obtained in Step 2 in 30 ml of a 10/3/1 mixture of tert-butanol/tetrahydrofuran/water there are added osmium tetroxide in the form of a 2.5% solution in 0.67 ml of 2-methyl-2-propanol and 1.35 mmol of 4-methylmorpholine-N-oxide monohydrate. After stirring for two days at ambient temperature, NaHSO3 solution is added. After stirring for one hour, the reaction mixture is extracted with dichloromethane. The organic phase is dried, filtered and then evaporated under reduced pressure. Chromatography of the residue over silica gel (dichloromethane/methanol: 98/2) allows the expected product to be isolated.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07056929B2
Quelldatensatzuspto-grants-2006_06
ORD IDord-f0249d5048814c81ab5e407120ad2ce7
Quellennotizuspto-grants-2006_06