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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49492Erstellt: 24. Oktober 2026

Water → 5-(Benzyloxy)-2,3-dihydro-1H-indole

https://huagongshe.com/de/reaction/49492

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt5-BenzyloxyindoleHCID 14624—
EduktPotassium HydroxideHCID 14797—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelAcetic AcidHCID 176—
Produkt5-(Benzyloxy)-2,3-dihydro-1H-indoleHCID 1679488189,2%

Reaktionsschritte

In analogy to the method described by Gordon W. Gribble, Joseph H. Hoffmann Synthesis 1977, 859-860, the following reaction was performed. To a precooled solution of 22.3 g (0.1 mol) 5-benzyloxyindole in 270 ml acetic acid, 19 g (0.3 mol) NaCNBH3 were added. The solution was stirred at RT for 2 h, the volume was reduced to one third and poured into 300 ml water. KOH was added under cooling and the solution was extracted with ether. The combined organic phases were washed with water, dried over Na2SO4 and evaporated to yield 20.1 g (89%) 5-Benzyloxy-2,3-dihydro-1H-indole as colorless oil, MS: 225 (M).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06706751B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-bd86c4538ce548e0b9203acfa8be0660
Quellennotizuspto-grants-2004_03