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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962810Generated: October 30, 2026

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

https://huagongshe.com/reaction/962810

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 L). The organic layer separated and washed with water, dried over anhydrous magnesium sulfate, filtered, and the solvent removed to afford an oil which solidies to afford 32.5 g (90.0%) a dark solid: mp 42°-43° C.; MS EI m/e 189/191 (M+); 1H NMR (CDCl3) δ 3.40-3.60 (2H, bs, NH2), 3.77 (2H, d, J=6 Hz), 4.14 (2H, d, J=6 Hz), 6.19-6.23 (1H, 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 numberUS05760070
Source datasetuspto-grants-1998_06
ORD IDord-c602332e747e4c78bb2c49ed70391033
Source noteuspto-grants-1998_06