Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826506Generated: October 27, 2026

Potassium Hydroxide → 3-Hexyl-6-methyl-6-(2-nitrophenyl)-3-azabicyclo[3.1.0]hexane-2,4-dione

https://huagongshe.com/reaction/1826506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant1-Hexyl-1H-pyrrole-2,4-dioneHCID 22141213—
Reactant[1-(2-Nitrophenyl)ethylidene]hydrazineHCID 59898054—
CatalystHCID 178418406HCID 178418406—
Solvent1,4-DioxaneHCID 31275—
Product3-Hexyl-6-methyl-6-(2-nitrophenyl)-3-azabicyclo[3.1.0]hexane-2,4-dioneHCID 2214118712%

Reaction Steps

To a solution of 1-(2-nitrophenyl)-1-ethanone hydrazone (Preparation 137, 4.00 g, 22.3 mmol) in dioxan (50 ml) was added manganese (IV) oxide (4.27 g, 49.2 mmol) followed by a saturated ethanolic solution of potassium hydroxide (2.0 ml), and the reaction mixture was stirred at room temperature for 4 h. The suspension was filtered through Celite™ washing with dioxan (ca. 150 ml) to give a deep red solution. 1-Hexyl-1H-pyrrole-2,4-dione (Preparation 56, 4.05 g, 22.4 mmol) was added to the solution and the reaction mixture was stirred at room temperature overnight before heating under reflux for 24 h. The reaction mixture was cooled to room temperature, filtered through Celite™ and concentrated in vacuo a crude dark brown oil. This was purified by chromatography in two batches using a Biotage Flash 40M™ cartridge packed with silica gel (90 g) eluting with dichloromethane:hexane (2:1) to afford an 8:1 exo:endo mixture of diastereomers of the title compound as a pale brown oil (880 mg, 12%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049444B2
Source datasetuspto-grants-2006_05
ORD IDord-c87d02d05adc4c7eaf46a2f802d1598c
Source noteuspto-grants-2006_05