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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366534Generated: October 25, 2026

Dimethylformamide → 3-n-Heptyl-3-azabicyclo[3.1.0]hexane-2,4-dione

https://huagongshe.com/reaction/366534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1-IodoheptaneHCID 20274—
ReactantSodium hydrideHCID 24758—
Reactant3-Azabicyclo[3.1.0]hexane-2,4-dioneHCID 3720053—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product3-n-Heptyl-3-azabicyclo[3.1.0]hexane-2,4-dioneHCID 23289980—

Reaction Steps

Sodium hydride (0.11 g) was added to a solution of 3-azabicyclo[3.1.0]hexane-2,4-dione (0.3 g) in dry tetrahydrofuran (10 ml) under a nitrogen atmosphere at room temperature. The suspension was stirred for 5 minutes and 1-iodoheptane (0.61 g) was then added in one portion to the reaction mixture. After stirring for two hours at room temperature, dimethylformamide (5 ml) was added and the reaction mixture was stirred for a further 16 hours at room temperature. The reaction mixture was diluted with dichloromethane and then partitioned with water (20 ml). The aqueous phase was extracted with dichloromethane (20 ml) and the combined organic extracts were washed with water (2×20 ml), dried (MgSO4) and evaporated in vacuo. The residue was purified by chromatography on silica gel (50 g) using 25-30% ethyl acetate/hexane as eluant to give the title compound as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130241
Source datasetuspto-grants-2000_10
ORD IDord-d7033219963e47e58c27ef5289b19e91
Source noteuspto-grants-2000_10