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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399012Generated: October 30, 2026

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

https://huagongshe.com/reaction/399012

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 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 numberUS05817690
Source datasetuspto-grants-1998_10
ORD IDord-15f7c081111b4a70be003d016246ccf2
Source noteuspto-grants-1998_10