Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704783Generated: October 30, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 178426239, compound

https://huagongshe.com/reaction/704783

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 178476609HCID 178476609—
SolventTolueneHCID 1140—
ProductHCID 178426239HCID 17842623958.5%

Reaction Steps

To a suspension of trans-3-acetoxy-4-(2-cyanoiminoimidazolidin-1-yl)-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-carbonitrile (0.35 g) in toluene (7 ml) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (0.19 ml) and the mixture was stirred under reflux for 2.5 hours. The solvent was evaporated in vacuo and the residue was dissolved in a mixture of ethyl acetate and water. The organic layer was separated, washed with brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residue was recrystallized from ethanol to give 4-(2-cyanoiminoimidazolidin-1-yl)-2,2-dimethyl-2H-1-benzopyran-6-carbonitrile (0.17 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988723
Source datasetuspto-grants-1991_01
ORD IDord-fb412fa564d84d598d9dcddd2b741430
Source noteuspto-grants-1991_01