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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366533Generated: October 25, 2026

1-Iodooctane → 3-Octyl-3-azabicyclo[3.1.0]hexane-2,4-dione

https://huagongshe.com/reaction/366533

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodooctaneHCID 12380—
ReactantSodium hydrideHCID 24758—
Reactant3-Azabicyclo[3.1.0]hexane-2,4-dioneHCID 3720053—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-Octyl-3-azabicyclo[3.1.0]hexane-2,4-dioneHCID 3796377—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (1.48 g, 60% in oil) was added to a stirred solution of 3-azabicyclo[3.1.0]hexane-2,4-dione (4.0 g) and 1-iodooctane (8.88 g) in dry dimethylformamide (70 ml) under a nitrogen atmosphere at 0° C. The reaction mixture was stirred at 0° C. for a further 30 minutes and then at room temperature for 16 hours. The mixture was diluted with water (100 ml) and then extracted with ether (150 ml). The organic extract was washed with water (2×70 ml), dried (MgSO4) and evaporated in vacuo to leave a brown oil. The oil was purified by distillation in vacuo (boiling point 146-147° C. @ 0.1 mmHg) to give the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130241
Source datasetuspto-grants-2000_10
ORD IDord-ce604a25f31d4f88833bc26b8a18e597
Source noteuspto-grants-2000_10