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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858367Generated: October 29, 2026

1-(2-Chloroethoxy)-2,6-dibromo-4-fluoro-3-nitrobenzene → 1-(2-Chloroethoxy)-4-fluoro-3-aminobenzene

https://huagongshe.com/reaction/1858367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Chloroethoxy)-2,6-dibromo-4-fluoro-3-nitrobenzeneHCID 10571629—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-(2-Chloroethoxy)-4-fluoro-3-aminobenzeneHCID 1058381590.2%

Reaction Steps

A solution of 1-(2-chloroethoxy)-2,6-dibromo-4-fluoro-3-nitrobenzene (73.2 g, 0.19 mol) in ethanol (1.1 L) containing 7.3 g of 10% palladium on carbon was hydrogenated at 40 psi for 5 days. The catalyst was filtered and the solvent was removed. The residue was dissolved in diethyl ether (300 ml) and washed with saturated aqueous sodium carbonate (200 ml). The organic layer was separated and washed with water, dried over anhydrous magnesium sulfate and filtered. The solvent was removed to afford an oil which solidified to afford 32.5 g (90.0%) of product as a dark solid: mp 42-43° C.; MS EI m/e 189/191 (M+); 1H NMR (CDCl3) δ3.40-3.60 (2H, bs, NH2), 3.77 (2H, d, J=6 Hz), 4.14 (2H, d, J=6 Hz), 6.19-6.23 (1 H, m), 6.36 (1H, dd, J=7, 3 Hz), 6.88 (1H, dd, J=11, 9 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150533
Source datasetuspto-grants-2000_11
ORD IDord-dac9aa4b5f5843ecbf704066bcada9f0
Source noteuspto-grants-2000_11