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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37702Erstellt: 25. Oktober 2026

Ethyl-1-propyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-acetate → Ethyl-1-propyl-1,3,4,9-tetrahydro-6-hydroxypyrano[3,4-b]indole-1-acetate

https://huagongshe.com/reaction/37702

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl-1-propyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-acetateHCID 19935728—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthanolHCID 702—
ProduktEthyl-1-propyl-1,3,4,9-tetrahydro-6-hydroxypyrano[3,4-b]indole-1-acetateHCID 1993574289,2%

Reaktionsschritte

A suspension of the 6-benzyloxypyranoindole (5.4 g, 13.25 mmol) of Step A, and 10% Pd/C catalyst (600 mg) in ethanol (150 mL) is hydrogenated for 6 hours in a Parr shaker. Filtration of the catalyst and evaporation of the solvent affords the title compound (3.75 g, 89%) as a cream-colored foam homogeneous by TLC.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05420289
Quelldatensatzuspto-grants-1995_05
ORD IDord-85a7e5c46b2c42ea8680c7c2812bb776
Quellennotizuspto-grants-1995_05