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HRID 547987Erstellt: 24. Oktober 2026

tert-Butyl hydroperoxide → 1H-Indene-2-carboxylic acid, 5-chloro-2,3-dihydro-2-hydroxy-1-oxo-, methyl ester

https://huagongshe.com/de/reaction/547987

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl hydroperoxideHCID 6410—
Edukt1H-Indene-2-carboxylic acid, 5-chloro-2,3-dihydro-1-oxo-, methyl esterHCID 11042391—
KatalysatorZirconium(4+) propan-2-olateHCID 3083750—
LösungsmittelTolueneHCID 1140—
LösungsmittelAcetonitrileHCID 6342—
Produkt1H-Indene-2-carboxylic acid, 5-chloro-2,3-dihydro-2-hydroxy-1-oxo-, methyl esterHCID 1097758589%

Reaktionsbedingungen

Temperatur30 °C

Reaktionsschritte

To a solution of methyl 5-chloro-2,3-dihydro-1-oxo-1H-indene-2-carboxylate (also known as methyl 5-chloro-1-oxo-2,3-dihydroindene-2-carboxylate) (0.500 g, 2.23 mmol) (Formula IIa wherein R1 is OCH3 and R4 is Cl) and zirconium(1V) isopropoxide (0.0086 g, 0.022 mmol) in toluene (1.34 g, 1.56 mL) at 30° C. was added an aqueous solution of tert-butyl hydroperoxide (70%, 0.316 g, 2.46 mmol). The reaction mixture was stirred for 24 hours at 30° C. and then diluted with acetonitrile (about 6 mL). Quantitative HPLC analysis showed 92% conversion of methyl 5-chloro-2,3-dihydro-1-oxo-1H-indene-2-carboxylate, forming racemic methyl 5-chloro-2,3-dihydro-2-hydroxy-1-oxo-1H-indene-2-carboxylate in 89% yield (97% chemoselectivity).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07939685B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-4932bb66191d4e22ae50ef1098387465
Quellennotizuspto-grants-2011_05