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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920988Generated: November 2, 2026

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

https://huagongshe.com/reaction/1920988

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 numberUS08173646B2
Source datasetuspto-grants-2012_05
ORD IDord-1c167eefa16f470bb643ce77246de2b4
Source noteuspto-grants-2012_05