HuagongsheHuagongshe Chemistry Print Report · For research reference only
ethyl 7-nitro-5-(trifluoromethoxy)-1H-indole-2-carboxylate → ethyl 7-amino-5-(trifluoromethoxy)-1H-indole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | ethyl 7-nitro-5-(trifluoromethoxy)-1H-indole-2-carboxylate | HCID 57476182 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl 7-amino-5-(trifluoromethoxy)-1H-indole-2-carboxylate | HCID 57476183 | 95% |
Reaction Steps
A mixture of ethyl 7-nitro-5-(trifluoromethoxy)-1H-indole-2-carboxylate (3.06 g), 10% palladium-carbon (50% containing water, 600 mg) and tetrahydrofuran (150 mL) was subjected to catalytic reduction under hydrogen atmosphere at normal pressure. The palladium-carbon was removed by filtration, and the filtrate was concentrated. The obtained crystals were washed with hexane to give the title compound (2.63 g, yield 95%) as colorless crystals. The crystals were recrystallized from ethyl acetate-hexane to give colorless prism crystals. melting point 190-191° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07652133B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-f7c1acfc8c7e4a10afe46d6eaf51c7af |
| Source note | uspto-grants-2010_01 |