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HRID 273218Erstellt: 25. Oktober 2026

Hydrochloric Acid → ethyl(6-bromo-1-oxo-2,3-dihydro-1H-inden-2-yl)acetate

https://huagongshe.com/reaction/273218

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthyl bromoacetateHCID 7748—
EduktDiisopropylamineHCID 7912—
EduktPotassium CarbonateHCID 11430—
Edukt1-Indanone, 6-bromo-HCID 139778—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produktethyl(6-bromo-1-oxo-2,3-dihydro-1H-inden-2-yl)acetateHCID 86592225—

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

n-Butyllithium (14 mL, 2 M in pentane) was added dropwise to a solution of diisopropylamine (2.86 g, 28 mmol) in tetrahydrofuran (60 mL) cooled to −70° C. After 30 minutes of stirring at −70° C., the mixture was treated with 6-bromo-1-indanone (4.8 g, 22.7 mmol), prepared according to the procedure described in J. Org. Chem., 49:4226-423 (1984), in two portions over 5 minutes. After 10 minutes, the mixture was allowed to warm to −50° C. and was treated with ethyl bromoacetate (4.8 g, 28 mmol). The mixture was allowed to warm to −10° C. and was stirred at −10 to −15° C. for 1 hour. The reaction was quenched by careful addition of water (60 mL) followed by isopropyl acetate (60 mL). The organic layer was separated, washed with aqueous HCl (50 mL, prepared by adjusting the pH of water to 2 with conc. HCl), and then aqueous potassium carbonate (50 mL, 5%). The organic layer was concentrated under vacuum to provide the title compound which was used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456196B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-581b20ae97d649d295c78b1ed3c6fe09
Quellennotizuspto-grants-2008_11