Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37694Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/37694

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBromhydrolHCID 166749—
EduktMethoxy indanoneHCID 10866644—
EduktDichloromethane ethylacetateHCID 21226138—
LösungsmittelBenzeneHCID 241—
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, dichloromethane-ethyl 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
PatentnummerUS05420289
Quelldatensatzuspto-grants-1995_05
ORD IDord-f438f32912d145acbeea5072e94ba4fd
Quellennotizuspto-grants-1995_05