Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423831Generated: October 27, 2026

2-Tert-butyl-4-(2-ethoxyphenyl)-5-nitrophenol → 2-Tert-butyl-4-(2-ethoxyphenyl)-5-aminophenol

https://huagongshe.com/reaction/423831

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Tert-butyl-4-(2-ethoxyphenyl)-5-nitrophenolHCID 57470240—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product2-Tert-butyl-4-(2-ethoxyphenyl)-5-aminophenolHCID 5747024292%

Reaction Steps

To a solution of 2-tert-butyl-4-(2-ethoxyphenyl)-5-nitrophenol (3.0 g, 9.5 mmol) in methanol (30 ml) was added Raney Ni (300 mg). The mixture was stirred under H2 (1 atm) at room temperature for 2 h. The catalyst was filtered off and the filtrate was concentrated. The residue was purified by column chromatography (petroleum ether-ethyl acetate, 6:1) to afford 2-tert-butyl-4-(2-ethoxyphenyl)-5-aminophenol (C-15) (2.35 g, 92%). 1HNMR (DMSO-d6) δ 8.89 (s, 1H), 7.19 (t, 1H,J=4.2 Hz), 7.10 (d, 1H,J=1.8 Hz), 7.08 (d, 1H,J=1.8 Hz), 6.94 (t, 1H,J=3.6 Hz), 6.67 (s, 1H), 6.16 (s, 1H), 4.25 (s, 1H), 4.00 (q, 2H,J=6.9 Hz), 1.26 (s, 9H), 1.21 (t, 3H,J=6.9 Hz); ESI-MS 286.0 m/z (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101767B2
Source datasetuspto-grants-2012_01
ORD IDord-15eeff082fc9490d85e9712df7ff0c1e
Source noteuspto-grants-2012_01