Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403890Generated: November 1, 2026

6-Tert-butoxy-2-tert-butyl-5-nitro-1H-indole → 6-tert-butoxy-2-tert-butyl-1H-indol-5-amine

https://huagongshe.com/reaction/1403890

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Tert-butoxy-2-tert-butyl-5-nitro-1H-indoleHCID 53421612—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product6-tert-butoxy-2-tert-butyl-1H-indol-5-amineHCID 5912915232%

Reaction Steps

A suspension of 6-tert-butoxy-2-tert-butyl-5-nitro-1H-indole (100 mg, 0.36 mmol) and Raney Ni (0.5 g) in MeOH (15 mL) was stirred under H2 atmosphere (1 atm) at the room temperature for 2.5 h. The catalyst was filtered off and the filtrate was concentrated under reduced pressure to dryness. The residue was recrystallized in ether to give 6-tert-butoxy-2-tert-butyl-1H-indol-5-amine (30 mg, 32%). 1H-NMR (300 MHz, MeOD) 6.98 (s, 1H), 6.90 (s, 1H), 5.94 (d, J=0.6 Hz, 1H), 1.42 (s, 9H), 1.36 (s, 9H); MS (ESI) m/e 205.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912199B2
Source datasetuspto-grants-2014_12
ORD IDord-839fe7db1ec44e278ff5278c89568c29
Source noteuspto-grants-2014_12