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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503322Generated: November 2, 2026

2-tert-Butyl-1-methyl-5-nitro-1H-indole → 2-tert-butyl-1-methyl-1H-indol-5-amine

https://huagongshe.com/reaction/503322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-tert-Butyl-1-methyl-5-nitro-1H-indoleHCID 53421182—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product2-tert-butyl-1-methyl-1H-indol-5-amineHCID 5912933066%

Reaction Steps

To a solution of 2-tert-butyl-1-methyl-5-nitro-1H-indole (3.00 g, 13.7 mmol) in MeOH (30 mL) was added Raney Ni (0.3 g) under nitrogen atmosphere. The mixture was stirred under hydrogen atmosphere (1 atm) at room temperature overnight. The mixture was filtered through a Celite pad and the filtrate was evaporated under vacuum. The crude residue was purified by column chromatography on silica gel (P.E/EtOAc 20:1) to give 2-tert-butyl-1-methyl-1H-indol-5-amine (1.7 g, 66%). 1H NMR (300 MHz, CDCl3) δ7.09 (d, J=8.4 Hz, 1H), 6.89-6.9 (m, 1H), 6.66 (dd, J=2.4, 8.7 Hz, 1H), 6.14 (d, J=0.6 Hz, 1H), 3.83 (s, 3H), 3.40 (brs, 2H), 1.45 (s, 9H); MS (ESI) m/e (M+H+) 203.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776905B2
Source datasetuspto-grants-2010_08
ORD IDord-688b9090adad44f887432fdbe556e184
Source noteuspto-grants-2010_08