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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761066Generated: November 1, 2026

Methyl iodide → methyl 4-methoxy-1-methyl-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1761066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactantmethyl 4-methoxy-1H-indole-2-carboxylateHCID 688172—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
Productmethyl 4-methoxy-1-methyl-1H-indole-2-carboxylateHCID 477790496.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

NaH (60% dispersion in mineral oil, 0.3 g, 7.3 mmole) was washed with hexane then suspended in anhydrous DMF (16 mL). The mixture was cooled to 0° C. and methyl 4-methoxy-1H-indol-2-carboxylate (1.0 g, 4.87 mmole) was added. The mixture was stirred under argon for 10 min, then MeI (1.3 mL, 20 mmole) was added, and the thick slurry was stirred at RT for 2.5 hr. The reaction was quenched with 10% NH4Cl (2 mL) and concentrated. The residue was partitioned between H2O and Et2O, and the organic layer was dried over MgSO4 and concentrated to yield the title compound (1.03 g, 96%) as a white solid: MS (ES) m/e 220.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06846819B1
Source datasetuspto-grants-2005_01
ORD IDord-2e208627ccef4a97be30d40c344c4cc2
Source noteuspto-grants-2005_01