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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468347Generated: October 30, 2026

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

https://huagongshe.com/reaction/468347

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 numberUS08623905B2
Source datasetuspto-grants-2014_01
ORD IDord-004483e9702c43c8a06e99a7e0c60600
Source noteuspto-grants-2014_01