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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20980Generated: October 26, 2026

Methyl iodide → 1-Methyl-1H-indole-6-carboxylic acid

https://huagongshe.com/reaction/20980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium hydrideHCID 24758—
Reactant1H-indole-6-carboxylic acidHCID 595230—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-Methyl-1H-indole-6-carboxylic acidHCID 19819261214.4%

Reaction Steps

In a similar manner to Step 1 of Reference Example 12, indole-6-carboxylic acid (200 mg, 1.24 mmol) was dissolved in DMF (2 mL), and the solution was treated with 60% sodium hydride-mineral oil dispersant (109 mg, 2.71 mmol), methyl iodide (0.258 mL, 0.410 mmol) and 4 mol/L aqueous potassium hydroxide solution (2 mL). The reaction mixture was added with water and separated into aqueous layer and organic layer, and the organic layer was removed. The aqueous layer was added with 1 mol/L hydrochloric acid to adjust the pH to 1, followed by stirring at room temperature for 1 hour. The obtained solid was collected by filtration and dried under reduced pressure to obtain 1-methylindole-6-carboxylic acid (154 mg, yield 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-a5aefe6165594ef5bfe0f2092a468033
Source noteuspto-grants-2010_06