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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1847387Generated: 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/1847387

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 numberUS08952050B2
Source datasetuspto-grants-2015_02
ORD IDord-1d77deb72906437195f696c868ae0eee
Source noteuspto-grants-2015_02