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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503342Generated: November 4, 2026

2-Tert-butyl-7-fluoro-5-nitro-1H-indole → 2-(Tert-butyl)-7-fluoro-1h-indol-5-amine

https://huagongshe.com/reaction/503342

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Tert-butyl-7-fluoro-5-nitro-1H-indoleHCID 53421189—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product2-(Tert-butyl)-7-fluoro-1h-indol-5-amineHCID 5135828331.4%

Reaction Steps

To a solution of 2-tert-butyl-7-fluoro-5-nitro-1H-indole (2.0 g, 8.5 mmol) in MeOH (20 mL) was added Ni (0.3 g) under nitrogen atmosphere. The reaction mixture was stirred under hydrogen atmosphere (1 atm) at room temperature overnight. The catalyst was filtered off through the celite pad and the filtrate was evaporated under vacuum. The crude product was purified by column chromatography on silica gel (petroleum ether/ethyl acetate 100:1) to give 2-tert-butyl-7-fluoro-1H-indol-5-amine (550 mg, 24%). 1H NMR (300 MHz, CDCl3) δ 7.87 (brs, 1H), 6.64 (d, J=1.5 Hz, 1H), 6.37 (dd, J=1.8, 12.3 Hz, 1H), 6.11 (dd, J=2.4, 3.6 Hz, 1H), 1.39 (s, 9H). MS (ESI) m/z (M+H+) 207.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776905B2
Source datasetuspto-grants-2010_08
ORD IDord-289f7971965948b69ba407d3e27f00db
Source noteuspto-grants-2010_08