HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964147Generated: October 25, 2026
Sodium Bicarbonate → ethyl 5-methoxy-4-methyl-1H-indole-2-carboxylate
https://huagongshe.com/reaction/1964147
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 4-bromo-5-methoxy-1H-indole-2-carboxylate | HCID 11460715 | — |
| Reactant | HCID 178477797 | HCID 178477797 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl 5-methoxy-4-methyl-1H-indole-2-carboxylate | HCID 21396313 | — |
Reaction Steps
To a reaction mixture of ethyl 4-bromo-5-methoxy-1H-indole-2-carboxylate (1 g, 3.35 mmol) and bis(tri-t-butylphosphine)palladium (0) (0.171 g, 0.335 mmol) in THF (10 mL) was added a 2 M solution of methylzinc(II) chloride in THF (5.03 mL, 10.06 mmol) at room temperature. The reaction was stirred at 65° C. for 2 h, cooled down, and added saturated aqueous NaHCO3 solution. The solid was filtered off through celite and washed with ethyl acetate. The filtrate was extracted with ethyl acetate. The combined organics were dried over anhydrous Na2SO4 and concentrated. The residue was purified by silica gel column chromatography to give the title compound as white solid (712 mg). LCMS m/z=234.2 [M+H]+; 1H NMR (400 MHz, CDCl3) δ ppm 1.42 (t, J=7.1 Hz, 3H), 2.44 (s, 3H), 3.87 (s, 3H), 4.41 (q, J=7.1 Hz, 2H), 7.05 (d, J=9.0 Hz, 1H), 7.19-7.24 (m, 2H), 8.81 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415484B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-84888d7bdf904eb2bf351d33cb69efa1 |
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| Source note | uspto-grants-2013_04 |
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