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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468202Generated: October 30, 2026

Sodium Carbonate → 5-Bromo-2-ethylaniline

https://huagongshe.com/reaction/468202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantStannous chloride dihydrateHCID 61436—
Reactant4-Bromo-1-ethyl-2-nitrobenzeneHCID 7566996—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-2-ethylanilineHCID 2334675617.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 2-ethyl-5-bromo-1-nitrobenzene (9.71 g, 230 mmol) in ethanol (125 ml) is added tin(II) chloride dihydrate (35.72 g, 225.71 mmol), followed by heating at 70° C. for 2 hours. After cooling to room temperature the solution is poured into crushed ice (1 liter) then diluted with ethyl acetate (200 ml). Solid sodium carbonate is cautiously added until pH 7 is achieved, at which stage the viscous mixture is filtered through diatomaceous earth (further washing with ethyl acetate/aqueous sodium carbonate) and the phases separated. After additional extraction of the aqueous phase, all organic phases are combined, dried over anhydrous magnesium sulfate then concentrated in vacuo. The crude oil is purified by flash column chromatography on silica gel (hexane/ethyl acetate 8:2 ratio) to afford 5-bromo-2-ethylaniline (7.89 g) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623907B2
Source datasetuspto-grants-2014_01
ORD IDord-64b041b9b31a4b2cb61052a71d6d304a
Source noteuspto-grants-2014_01