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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40061Generated: October 26, 2026

Benzyl Bromide → Ethyl1-Benzyl-3-formyl-2-isopropyl-1H-indole-6-carboxylate

https://huagongshe.com/reaction/40061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl3-Formyl-2-isopropyl-1H-indole-6-carboxylateHCID 59762423—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductEthyl1-Benzyl-3-formyl-2-isopropyl-1H-indole-6-carboxylateHCID 59762439—

Reaction Steps

General Procedure C. To a solution of ethyl3-formyl-2-isopropyl-1H-indole-6-carboxylate (Compound 34, 2.08 g, 8.04 mmol) in DMF (15 ml) was added K2CO3 (3.32 g, 24.1 mmol) and benzyl bromide (1.91 ml, 16.1 mmol). The reaction was stirred at room temperature for 12 h, diluted with EtOAc, washed with H2O, brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→35% EtOAc-hexanes) to yield the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524917B2
Source datasetuspto-grants-2013_09
ORD IDord-c247067584fa4437babf8edaa82225a9
Source noteuspto-grants-2013_09