HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826990Generated: October 25, 2026
Dimethyl oxalate → 7-Benzyloxy-1-methylindole
https://huagongshe.com/reaction/1826990
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl oxalate | HCID 11120 | — |
| Reactant | 7-(Benzyloxy)-1H-indole | HCID 260798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-methyl-1H-indol-7-ol | HCID 22136802 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Benzyloxy-1-methylindole | HCID 22136813 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07053117B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-35e34d7e070f47b8a7d4bdd0f163d079 |
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| Source note | uspto-grants-2006_05 |
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