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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470048Generated: October 30, 2026

2-Tert-butyl-4-bromo-5-nitrophenol → 2-Tert-butyl-4-bromo-5-amino-phenol

https://huagongshe.com/reaction/470048

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Tert-butyl-4-bromo-5-nitrophenolHCID 57470236—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product2-Tert-butyl-4-bromo-5-amino-phenolHCID 5747024870%

Reaction Steps

To a solution of 2-tert-butyl-4-bromo-5-nitrophenol (C-14-a) (12 g, 43.8 mmol) in MeOH (90 mL) was added Ni (2.4 g). The reaction mixture was stirred under H2 (1 atm) for 4 h. The mixture was filtered and the filtrate was concentrated. The crude product was recrystallized from ethyl acetate and petroleum ether to give 2-tert-butyl-4-bromo-5-amino-phenol (C-27) (7.2 g, 70%). 1H NMR (DMSO-d6) δ 9.15 (s, 1 H), 6.91 (s, 1 H), 6.24 (s, 1 H), 4.90 (br s, 2 H), 1.22 (s, 9 H); ESI-MS 244.0 m/z (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629162B2
Source datasetuspto-grants-2014_01
ORD IDord-286bcb5afe8d42d1b69e94428ecc0e4b
Source noteuspto-grants-2014_01