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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23458Generated: October 26, 2026

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

https://huagongshe.com/reaction/23458

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 numberUS06852711B2
Source datasetuspto-grants-2005_02
ORD IDord-d7f5f06869914232b71e686a20541302
Source noteuspto-grants-2005_02