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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859531Generated: October 27, 2026

1-Bromo-4-tert-butyl-2-nitrobenzene → 3-tert-Butylaniline

https://huagongshe.com/reaction/1859531

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-tert-butyl-2-nitrobenzeneHCID 11253906—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-tert-ButylanilineHCID 79334—

Reaction Steps

1-Bromo-4-tert-butyl-2-nitro-benzene (18 g) was reduced as described in General Method 3 using 10% palladium on charcoal (1 g) and MeOH (100 mL) in a hydrogen atmosphere (50 psi). The catalyst was filtered, and the solvents were evaporated. The residue was taken in EtOAc (100 mL) and washed with saturated sodium bicarbonate solution and H2O. The solution was dried and concentrated. The residue was purified by flash chromatography to give 3-tert-butyl-phenylamine. MS (APCI): 150 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528510B1
Source datasetuspto-grants-2003_03
ORD IDord-10a94bc5a0604676870016b3681d7e2b
Source noteuspto-grants-2003_03