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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164955Generated: November 2, 2026

Diethylamine → HCID 19863387, compound

https://huagongshe.com/reaction/1164955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
Reactant1-(3-Chloropropoxy)-4-nitrobenzeneHCID 11844617—
SolventAcetonitrileHCID 6342—
ProductHCID 19863387HCID 19863387—

Reaction Steps

Heat 19.41 g (0.09 mol) of 1-(3-chloropropoxy)-4-nitrobenzene and 50 mL (0.48 mol) of diethylamine in 100 mL of acetonitrile at 45°-50° C. Follow the progress of the reaction by thin-layer chromatography on silica gel (acetonitrile:ammonium hydroxide, 95:5). At the completion of the reaction remove the solvent in vacuo. Dissolve the residue in 100 mL of H2O and make the mixture acidic (pH=1) with concentrated hydrochloric acid. Extract the acidic solution with 3×100 mL of diethyl ether. Neutralize the acid solution (pH=7) with 20% aqueous sodium hydroxide solution and extract with 3×100 mL of diethyl ether. Adjust the pH of the aqueous layer to 12 with 20% aqueous sodium hydroxide solution and extract with 3×100 mL of diethyl ether. Wash the ether extracts from the basic solution with 50 mL of saturated sodium chloride solution, combine them and dry over anhydrous sodium sulfate. Remove the drying agent by filtration and evaporate the solvent in vacuo. Dissolve the residue in 100 mL of methanol and add concentrated hydrochloric acid until pH=1. Stir the solution with 2 g of charcoal, filter and remove the solvent in vacuo. Recrystallize the residue from acetonitrile to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906634
Source datasetuspto-grants-1990_03
ORD IDord-729712d3322b4139bfb1917f8365a52f
Source noteuspto-grants-1990_03