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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646120Generated: October 30, 2026

1-Bromo-4-nitrobenzene → 5-(4-tert-Butylphenyl)-1-(4-nitrophenyl)indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/646120

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-nitrobenzeneHCID 11466—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 5-(4-(tert-butyl)phenyl)-1H-indole-2-carboxylateHCID 68475095—
Solvent1,4-DioxaneHCID 31275—
Product5-(4-tert-Butylphenyl)-1-(4-nitrophenyl)indole-2-carboxylic acid ethyl esterHCID 68695069—
ProductSodium 5-(4-tert-butylphenyl)-1-(4-nitrophenyl)indole-2-carboxylateHCID 68701941—

Reaction Steps

5-(4-tert-Butylphenyl)-1-(4-nitrophenyl)indole-2-carboxylic acid ethyl ester was prepared in accordance with Example 1 using 5-(4-tert-butylphenyl)indole-2-carboxylic acid ethyl ester and 1-bromo-4-nitrobenzene. This ester (207 mg, 0.47 mmol) was dissolved in dioxane (2 mL) to which aqueous NaOH (1M, 1 mL) was added. The mixture was heated using microwave irradiation at 120° C. for 15 min and allowed to cool. The precipitate was filtered off, washed with water and recrystallised from EtOH/EtOAc to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705023B2
Source datasetuspto-grants-2010_04
ORD IDord-6189d39c193b4266b377ce637ba4368b
Source noteuspto-grants-2010_04