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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416613Generated: October 28, 2026

Ethylenediamine → Ammonia

https://huagongshe.com/reaction/2416613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantSodium HydroxideHCID 14798—
Reactant3,5-DichloropyridineHCID 17153—
ReactantSodiumHCID 5360545—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductAmmoniaHCID 222—
ProductHCID 22478580HCID 22478580—

Reaction Conditions

Temperature70 °C

Reaction Steps

Sodium (4.98 g, 216.7 mmol) was added to methanol (100 ml), and was allowed to react, the mixture was evaporated. 3.5-Dichloropyridine (25.0 g, 166.7 mmol) and dimethyl sulfoxide (250 ml) were added. The mixture was stirred at 70° C. overnight. Aqueous sodium hydroxide (500 ml, 1 M) was added, and the mixture was extracted twice with diethyl ether (500 ml). The crude mixture was stirred together with ethylenediamine (50.0 g, 833.5 mmol), potassium tert-butoxide (37.4 g, 333.4 mmol) and 1,2-dimethoxyethane (500 ml) at reflux for 4 h. Aqueous sodium hydroxide (1 l, 1 M) was added, and the mixture was extracted five times with ethyl acetate (500 ml). Chromatography on silica gel with dichloromethane, methanol and conc. ammonia (89:10:1) gave the title compound as free base. Yield 13.0 g, 47%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825189B1
Source datasetuspto-grants-2004_11
ORD IDord-f9e99c57c5514b1cb229484f8a0e12ab
Source noteuspto-grants-2004_11