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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206465Generated: October 27, 2026

(1-Bromoethyl)benzene → ethyl 2-methyl-1-(1-phenylethyl)-1H-indole-3-carboxylate

https://huagongshe.com/reaction/2206465

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1-Bromoethyl)benzeneHCID 11454—
ReactantSodium hydrideHCID 24758—
Reactantethyl 2-methyl-1H-indole-3-carboxylateHCID 4072358—
SolventDimethylformamideHCID 6228—
Productethyl 2-methyl-1-(1-phenylethyl)-1H-indole-3-carboxylateHCID 8974022056.1%

Reaction Steps

A mixture of ethyl 2-methyl-1H-indole-3-carboxylate (400 mg, 1.97 mmol) and sodium hydride (47 mg, 2.0 mmol) in N,N-dimethylformamide (5.0 mL) was stirred at room temperature for 0.5 hours, and then (1-bromoethyl)benzene (361 mg, 2.0 mmol) was added. The mixture was stirred at room temperature for 3 hours. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. Organic layers were combined and concentrated to give a residue. The residue was purified by chromatography (petroleum ether/ethyl acetate 5:1) to give ethyl 2-methyl-1-(1-phenylethyl)-1H-indole-3-carboxylate (340 mg, 56%). LRMS (M+H+) m/z: calcd 307.16. found 307.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371331B2
Source datasetuspto-grants-2016_06
ORD IDord-824e13e84ae64d5f94a0eee41f3512dc
Source noteuspto-grants-2016_06