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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 484241Erstellt: 24. Oktober 2026

Acetate → 6-Hydroxy-2-methyl-2,3-dihydro-1h-inden-1-one

https://huagongshe.com/de/reaction/484241

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetateHCID 175—
EduktBenzeneHCID 241—
EduktHydrochloric AcidHCID 313—
EduktBromhydrolHCID 166749—
EduktMethoxy indanoneHCID 10866644—
Produkt6-Hydroxy-2-methyl-2,3-dihydro-1h-inden-1-oneHCID 234338—

Reaktionsschritte

To a stirred solution of anhydrous aluminum bromide (69.82 g, 0.261 mole) in anhydrous benzene (250 mL) kept under nitrogen is added dropwise over 30 minutes a solution of the methoxy indanone (18 g, 0.102 mole) of Step C, in benzene (60 mL). The mixture is gently refluxed for 3 hours (TLC, dichloromethaneethyl acetate 8:2, UV), cooled in an ice bath and treated dropwise with 6N-HCl (ca. 200 mL) to decompose the aluminum complex. The aqueous phase is extracted with ether (3 times), the extracts are concentrated at reduced pressure and extracted with 2.5N-NaOH (2×75 mL and 1×50 mL). The basic extracts are neutralized (ice bath) with concentrated HCl and the oil that separates is extracted with ether (3 times). The combined extracts are washed with brine, dried (MgSO4) and evaporated to yield an oil that readily solidifies. The crude material is flash chromatographed (on silica Merck-60, gradient CH2Cl2, CH2Cl2 -ethyl acetate 85:15 ) to provide the pure title compound (13.60 g, nearly colorless solid, 82%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05229516
Quelldatensatzuspto-grants-1993_07
ORD IDord-1245027b22874090b07ae6a4bca50ccb
Quellennotizuspto-grants-1993_07