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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372695Generated: October 31, 2026

Water → Methyl 1-benzylindole-3-carboxylate

https://huagongshe.com/reaction/1372695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantMethyl indole-3-carboxylateHCID 589098—
SolventDimethylformamideHCID 6228—
ProductMethyl 1-benzylindole-3-carboxylateHCID 952042100%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (60% in oil, 274.1 mg, 6.853 mmol) was suspended in DMF (8.0 ml). To the resulting suspension was added methyl indole-3-carboxylate (400.2 mg, 2.284 mmol) under stirring at 0° C., followed by stirring at the same temperature for 30 minutes. To the reaction mixture was added benzyl bromide (0.41 ml, 3.427 mmol) at 0° C. After stirring at room temperature for 1 hour, the reaction mixture was added with water to terminate the reaction. The reaction mixture was then extracted with ethyl acetate. The extract was washed with 1N HCl, 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 (6:1, v/v) eluate fractions, methyl 1-benzylindole-3-carboxylate (100%) was obtained as a gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-b69d27407e3a4376a7ff4abfcc70a09b
Source noteuspto-grants-2007_01