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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015441Generated: October 30, 2026

Methyl iodide → Methyl 3-(methoxymethyl)-1H-indole-5-carboxylate

https://huagongshe.com/reaction/1015441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantMethyl 3-(hydroxymethyl)-1H-indole-5-carboxylateHCID 67300394—
CatalystSilver(II) oxideHCID 92152—
SolventAcetonitrileHCID 6342—
ProductMethyl 3-(methoxymethyl)-1H-indole-5-carboxylateHCID 67300506—

Reaction Conditions

Temperature80 °C

Reaction Steps

A 327 mg portion of methyl 3-(hydroxymethyl)-1H-indole-5-carboxylate was dissolved in 9 ml of acetonitrile, mixed with 385 mg of silver oxide and 3.6 ml of methyl iodide and stirred at 80° C. for 5 hours. A 385 mg portion of silver oxide was further added thereto and stirred overnight at 80° C. A 385 mg portion of silver oxide and 3.6 ml of methyl iodide were further added thereto and stirred at 80° C. for 9 hours. After cooling to room temperature, the insoluble matter was removed, the solvent was evaporated, and then the residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:6 to 1:5 to 1:4) to obtain 143 mg of methyl 3-(methoxymethyl)-1H-indole-5-carboxylate as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985764B2
Source datasetuspto-grants-2011_07
ORD IDord-71d787d2a80b42b096f37d813ecec770
Source noteuspto-grants-2011_07