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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826990Generated: October 25, 2026

Dimethyl oxalate → 7-Benzyloxy-1-methylindole

https://huagongshe.com/reaction/1826990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl oxalateHCID 11120—
Reactant7-(Benzyloxy)-1H-indoleHCID 260798—
ReactantSodium BicarbonateHCID 516892—
Reactant1-methyl-1H-indol-7-olHCID 22136802—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Product7-Benzyloxy-1-methylindoleHCID 22136813—

Reaction Conditions

Temperature110 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053117B2
Source datasetuspto-grants-2006_05
ORD IDord-35e34d7e070f47b8a7d4bdd0f163d079
Source noteuspto-grants-2006_05