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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071796Generated: October 26, 2026

Methyl iodide → 1-Methyl-indole-2,5-dicarboxylic acid diethyl ester

https://huagongshe.com/reaction/1071796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactantdiethyl 1H-indole-2,5-dicarboxylateHCID 15629756—
SolventDimethylformamideHCID 6228—
Product1-Methyl-indole-2,5-dicarboxylic acid diethyl esterHCID 6755017997%

Reaction Steps

Sodium hydride (60%-suspension, 144 mg, 3.6 mmole) was added to a stirred solution of 1H-indole-2,5-dicarboxylic acid diethyl ester 16 (784 mg, 3.0 mmole) in dry DMF (15.0 ml) and kept at ambient temperature for 30 min. To a resulted reaction mixture MeI (280 μl, 4.5 mmol) was added and kept at ambient temperature for 16 hours and evaporated. The residue was suspended in AcOEt (100 ml) and washed with water (2×20 ml), 0.01 M HCl (3×20 ml) and brine (2×100 ml). The organic layer was dried over sodium sulfate and evaporated to give 800 mg (97%) of 1-methyl-indole-2,5-dicarboxylic acid diethyl ester 17 as a yellow oil. 1H-NMR (DMSO-d6): 8.45 (m, 1H, H-4, indole); 8.03 (m, 1H, H-6, indole); 7.40 (m, 11H, H-7, indole); 7.38 (s, 1H, H-3, indole); 4.40 (m, 4H, —OCH2CH3); 4.10 (s, 3H, NCH3, indole); 1.42 (m, 4H, —OCH2CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906103B2
Source datasetuspto-grants-2005_06
ORD IDord-9920ffdb7b7f4c6e80e69b1f6d13a09f
Source noteuspto-grants-2005_06