Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037941Generated: November 1, 2026

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

https://huagongshe.com/reaction/2037941

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) δ 7.09 (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 numberUS08575209B2
Source datasetuspto-grants-2013_11
ORD IDord-572f9655752149dd940021069da12dff
Source noteuspto-grants-2013_11