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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908432Generated: October 28, 2026

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

https://huagongshe.com/reaction/1908432

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 numberUS08598181B2
Source datasetuspto-grants-2013_12
ORD IDord-a06cf67437b141158b2b861c8ff229a0
Source noteuspto-grants-2013_12