Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542209Generated: November 1, 2026

Diethyl Ether → HCID 131715090, compound

https://huagongshe.com/reaction/542209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13359982HCID 13359982—
CatalystZincchlorideHCID 3007855—
SolventDimethylacetamideHCID 31374—
ProductHCID 131715090HCID 131715090—

Reaction Steps

N-[1-(4-Benzylpiperazin-1-yl)ethylidene]-2-cyano-4,5-dimethoxyaniline (13.5 g) and zinc chloride (4.86 g) in dimethylacetamide (90 ml) were stirred under reflux for 21/2 hours; further zinc chloride (0.5, 0.2 g) was added after 1/2 and 11/2 hours respectively. The mixture was cooled, treated with ether (700 ml, 2×100 ml) and the supernatant discarded each time. The residual tar was then treated with sodium hydroxide solution (2N, 100 ml) and methylene chloride (100 ml) and the mixture was stirred at room temperature for 5 minutes. The organic layer was separated, the aqueous phase extracted with methylene chloride and the total organic extracts washed with water. The dried (Na2SO4) extracts were evaporated in vacuo and the brown residue (~13 g) purified by chromatography on silica gel (Merck 9385, 250 g) eluting with chloroform-methanol (100:0→88:12). A sample of the pure product (6.95 g) was taken up in ethanol, treated with ethereal hydrogen chloride and evaporated in vacuo. The residue was recrystallised from methanol to give 4-amino-6,7-dimethoxy-2(4-benzylpiperazin-1-yl)quinoline dihydrochloride sesquihydrate, m.p. 260°-263°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04656174
Source datasetuspto-grants-1987_04
ORD IDord-dc89b541f99c46e08cd5a1ed7a6fb618
Source noteuspto-grants-1987_04