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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740302Generated: October 31, 2026

Indole → HCID 21838287, compound

https://huagongshe.com/reaction/1740302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantSodiumHCID 5360545—
ReactantHCID 21838243HCID 21838243—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
ProductHCID 21838287HCID 21838287—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of sodium hydride (0.20 g) in anhydrous toluene (23 ml) was added a hot solution of methyl 3-(indol-4-yl)benzoate (1.16 g) in toluene (5.8 ml). Since a sodium salt did not form, N,N-dimethylformamide (0.5 ml) was introduced. An evolution of gas occurred with the formation of the orange sodium salt of the indole. After being stirred for 20 minutes methyl iodide was added thereto and the mixture was stirred at 60° C. for four hours. Then the sodium iodide was filtered off and washed with toluene. The filtrate was concentrated under reduced pressure and the residue was purified by column chromatography on silica gel eluting with a mixture of hexane and acetone (20:1) to afford methyl 3-(1-methylindol-4-yl)benzoate (0.35 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05968985
Source datasetuspto-grants-1999_10
ORD IDord-c6d43e39c1dd4f968ddfd40af0751afb
Source noteuspto-grants-1999_10