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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39194Generated: October 29, 2026

2-Bromo-1-ethyl-4-nitrobenzene → 3-Bromo-4-ethylaniline

https://huagongshe.com/reaction/39194

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-ethyl-4-nitrobenzeneHCID 22345594—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product3-Bromo-4-ethylanilineHCID 22345617210.4%

Reaction Steps

To a solution of 2-bromo-1-ethyl-4-nitro-benzene (25 g, 0.019 mol) in MeOH (100 mL) was added Raney-Ni (2.5 g). The reaction mixture was hydrogenated under hydrogen (1 atm) at room temperature. After stirring for 3 hours, the mixture was filtered and concentrated under reduced pressure. The crude material was purified by preparative HPLC to give 3-bromo-4-ethylaniline (8.0 g, 48%). 1H NMR (400 MHz, CDCl3) δ 6.92 (d, J=8.4 Hz, 1H), 6.83 (d, J=2.4 Hz, 1H), 6.52 (dd, J=2.4, 8.4 Hz, 1H), 2.57 (q, J=7.6 Hz, 2H), 1.10 (t, J=7.6 Hz, 3H). MS (ESI) m/e (M+H+) 200.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524767B2
Source datasetuspto-grants-2013_09
ORD IDord-bb43985f953642729fb45522e2dca988
Source noteuspto-grants-2013_09