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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994798Generated: October 30, 2026

ethyl 7-nitro-5-(trifluoromethoxy)-1H-indole-2-carboxylate → ethyl 7-amino-5-(trifluoromethoxy)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1994798

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 7-nitro-5-(trifluoromethoxy)-1H-indole-2-carboxylateHCID 57476182—
CatalystHCID 178418390HCID 178418390—
SolventTetrahydrofuranHCID 8028—
Productethyl 7-amino-5-(trifluoromethoxy)-1H-indole-2-carboxylateHCID 5747618395%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652133B2
Source datasetuspto-grants-2010_01
ORD IDord-f7c1acfc8c7e4a10afe46d6eaf51c7af
Source noteuspto-grants-2010_01