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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503313Generated: October 30, 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/503313

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 numberUS07776905B2
Source datasetuspto-grants-2010_08
ORD IDord-65dba9012157466b82afae136ba95f9f
Source noteuspto-grants-2010_08