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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1826990Erstellt: 26. Oktober 2026

Dimethyl oxalate → 7-Benzyloxy-1-methylindole

https://huagongshe.com/reaction/1826990

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl oxalateHCID 11120—
Edukt7-(Benzyloxy)-1H-indoleHCID 260798—
EduktSodium BicarbonateHCID 516892—
Edukt1-methyl-1H-indol-7-olHCID 22136802—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelDimethylformamideHCID 6228—
Produkt7-Benzyloxy-1-methylindoleHCID 22136813—

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

1-Methyl-indol-7-ol: A mixture of 7-benzyloxyindole (300 mg, 1.34 mmol), dimethyl oxalate (317 mg, 2.68 mmol) and potassium tert-butoxide (302 mg, 2.68 mmol) in 5 mL DMF was stirred at 110° C. overnight. The solution was poured into NaHCO3 saturated solution (20 mL) and extracted with EtOAc. The organic layer was separated, washed with brine and dried over Na2SO4. The solvent was removed in vacuo to yield 200 mg of 7-benzyloxy-1-methylindole, which was hydrogenated by 5% Pd/C in 20 mL methanol under H2 (50 psi) to yield 90 mg (45.5%) of the title compound. 1H NMR (CDCl3): 7.19–7.16 (m, 1H), 6.94 (d, J=3 Hz, 1H), 6.86 (t, J=7.5 Hz, 1H), 6.48–6.46 (m, 1H), 6.40 (d, J=3 Hz, 1H), 5.05 (s, 1H), 4.07 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07053117B2
Quelldatensatzuspto-grants-2006_05
ORD IDord-35e34d7e070f47b8a7d4bdd0f163d079
Quellennotizuspto-grants-2006_05