Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225862Generated: October 27, 2026

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

https://huagongshe.com/reaction/225862

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, 03 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 numberUS07557125B2
Source datasetuspto-grants-2009_07
ORD IDord-dc808ffbce5b4b6bad862c0ffa2258ee
Source noteuspto-grants-2009_07