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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401302Generated: October 30, 2026

Ammonium formate → 5-Amino-2-(tert-butyl)phenol

https://huagongshe.com/reaction/401302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant2-Tert-butyl-5-nitrophenolHCID 21959617—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product5-Amino-2-(tert-butyl)phenolHCID 5747020987.2%

Reaction Steps

To a refluxing solution of 2-tert-butyl-5-nitrophenol (C-1-a) (196 mg, 1.0 mmol) in EtOH (10 mL) was added ammonium formate (200 mg, 3.1 mmol), followed by 140 mg of 10% Pd—C. The reaction mixture was refluxed for additional 30 min, cooled to room temperature and filtered through a plug of Celite. The filtrate was concentrated to dryness and purified by column chromatography (20-30% EtOAc-Hexane) to give 2-tert-butyl-5-aminophenol (C-1) (144 mg, 87%). 1H NMR (400 MHz, DMSO-d6) δ 8.76 (s, 1H), 6.74 (d, J=8.3 Hz, 1H), 6.04 (d, J=2.3 Hz, 1H), 5.93 (dd, J=8.2, 2.3 Hz, 1H), 4.67 (s, 2H), 1.26 (s, 9H); HPLC ret. time 2.26 min, 10-99% CH3CN, 5 min run; ESI-MS 166.1 m/z (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741925B2
Source datasetuspto-grants-2014_06
ORD IDord-7f275479cb8f48e7b9a0ade0d96f0cb1
Source noteuspto-grants-2014_06