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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901441Generated: October 30, 2026

Potassium Carbonate → HCID 15838022, compound

https://huagongshe.com/reaction/1901441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant1-Bromo-4-chlorobutaneHCID 81364—
ReactantHCID 178516734HCID 178516734—
SolventDimethylformamideHCID 6228—
ProductHCID 15838022HCID 1583802254.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

300 mg (2 mmol) of 2-hydroxy-5,6,7,8-tetrahydroquinoxaline was dissolved in 5 ml of DMF, and 360 μl (2.4 mmol) of 1,8-diazabicyclo[5.4.0]undeca-7-ene (DBU) and 277 μl (2.4 mmol) of 1-bromo-4-chlorobutane were added thereto. The resultant mixture was stirred with heating at 60° C. for 22 hours to effect a reaction. The DMF in the resultant reaction mixture was distilled off in vacuo to thereby obtain a residue. An aqueous solution of potassium carbonate was added to the obtained residue, followed by extraction with chloroform to obtain an extract. The extract was dried over sodium sulfate anhydride, and subjected to filtration to thereby obtain a filtrate. The solvent of the filtrate was distilled off to thereby obtain a residue. The obtained residue was purified by silica gel column chromatography. That is, the residue was charged in a column of 20 g of silica gel (Art7734, manufactured and sold by E. Merck, Darmstadt) and eluted with chloroform, to thereby obtain 263 mg of 2-(4-chlorobutoxy)-5,6,7,8-tetrahydroquinoxaline (yield: 54.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578596
Source datasetuspto-grants-1996_11
ORD IDord-4aba6d5eb4d647e185d3fd47596b501a
Source noteuspto-grants-1996_11