HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-4-nitrobenzene → 5-(4-tert-Butylphenyl)-1-(4-nitrophenyl)indole-2-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-4-nitrobenzene | HCID 11466 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 5-(4-(tert-butyl)phenyl)-1H-indole-2-carboxylate | HCID 68475095 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(4-tert-Butylphenyl)-1-(4-nitrophenyl)indole-2-carboxylic acid ethyl ester | HCID 68695069 | — |
| Product | Sodium 5-(4-tert-butylphenyl)-1-(4-nitrophenyl)indole-2-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07705023B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-6189d39c193b4266b377ce637ba4368b |
| Source note | uspto-grants-2010_04 |