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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 4-bromo-5-methoxy-1H-indole-2-carboxylateHCID 11460715—
ReactantHCID 178477797HCID 178477797—
CatalystHCID 178418851HCID 178418851—
SolventTetrahydrofuranHCID 8028—
Productethyl 5-methoxy-4-methyl-1H-indole-2-carboxylateHCID 21396313—

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415484B2
Source datasetuspto-grants-2013_04
ORD IDord-84888d7bdf904eb2bf351d33cb69efa1
Source noteuspto-grants-2013_04