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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 414414Erstellt: 26. Oktober 2026

Hydrochloric Acid → 1-(2,3-Dihydro-1H-indol-7-yl)ethan-1-one

https://huagongshe.com/reaction/414414

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktWaterHCID 962—
EduktAcetonitrileHCID 6342—
EduktIndolineHCID 10328—
EduktBoron tribromideHCID 25134—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelTolueneHCID 1140—
Produkt1-(2,3-Dihydro-1H-indol-7-yl)ethan-1-oneHCID 13699421—

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

To a solution of 47.35 g. (0.5 mole) of boron tribromide in 300 ml. of toluene at 0° C. was added dropwise a solution of 50 g. (0.42 mole) of indoline and 22.39 g. (0.546 mole) of acetonitrile in 200 ml. of toluene. After stirring for 10 minutes 67.2 g. (0.5 mole) of aluminum chloride was added in portions. The resulting reaction mixture was heated to reflux for 66 hours, cooled to 5° C. and treated with 80 ml. of water and 330 ml. of 2N hydrochloric acid. The resulting mixture was heated to reflux for 2.5 hours, cooled and filtered. The filtrate was set aside and the solids suspended in 500 ml. of water and treated with 2N sodium hydroxide solution until basic. The basic mixture wa extracted (2×200 ml.) with methylene chloride and the organic phase separated, dried and concentrated to a solid, 17.2 g. The filtrate which was set aside was made basic with 4N aqueous sodium hydroxide and extracted with methylene chloride. The organic phase was separated, dried and concentrated to a solid, 21.8 g. The combined solids were recrystallized from hexane, 30 g., m.p. 83°-85° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04791129
Quelldatensatzuspto-grants-1988_12
ORD IDord-ac44012fb0834c0b9ac3d45f9787f0a1
Quellennotizuspto-grants-1988_12