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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372691Generated: October 31, 2026

Water → Methyl 1-(1-methylethyl)-1H-indole-3-carboxylate

https://huagongshe.com/reaction/1372691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsopropyl iodideHCID 6362—
ReactantSodium hydrideHCID 24758—
ReactantMethyl indole-3-carboxylateHCID 589098—
SolventDimethylformamideHCID 6228—
ProductMethyl 1-(1-methylethyl)-1H-indole-3-carboxylateHCID 1044334278%

Reaction Steps

In DMF (8.0 ml) was suspended sodium hydride (60% in oil, 275.2 mg, 6.881 mmol). To the resulting suspension was added methyl indole-3-carboxylate (401.8 mg, 2.294 mmol) at 0° C. under stirring. After stirring for further 45 minutes at the same temperature, isopropyl iodide (0.34 ml, 3.440 mmol) was added to the reaction mixture. Stirring was then conducted for 1.5 hours at 0° C. and for 7 hours at room temperature. Water was added to the reaction mixture to terminate the reaction, followed by extraction with ethyl acetate. The extract was washed successively with 1N HCl and saturated saline, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from hexane-ethyl acetate (3:1, v/v) eluate fractions, methyl 1-isopropylindole-3-carboxylate (387.6 mg, 78%) was obtained as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-6f51e8baaa8a47e393f5c62643d31f7e
Source noteuspto-grants-2007_01