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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276890Generated: November 3, 2026

1,4-Dioxane → 2a-(3-Formylpropyl)-2a,3,4,5-tetrahydro-1H-benz[cd]indol-2-one

https://huagongshe.com/reaction/276890

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantMethyl morpholine oxideHCID 82029—
Reactant2a-(4-Pentenyl)-2a,3,4,5-tetrahydrobenzo[cd]indol-2(1H)-oneHCID 373266—
ReactantSodium periodateHCID 23667635—
CatalystOsmium TetroxideHCID 30318—
SolventWaterHCID 962—
Product2a-(3-Formylpropyl)-2a,3,4,5-tetrahydro-1H-benz[cd]indol-2-oneHCID 15542636100.8%

Reaction Steps

In a shaded container, 2a-(4-pentenyl)-2a,3,4,5-tetrahydrobenz[cd]indole-2(1H)-one (1.3 g, 5.3 mmol) and N-methylmorpholine oxide (1.9 g, 16 mmol) were dissolved in a mixed solvent of 1,4-dioxane (20 ml) and water (10 ml), and the resulting solution was mixed with osmium tetroxide (4% aqueous solution 3.4 ml, 0.53 mmol) and stirred at a room temperature for 2 hours. The reaction solution was mixed with water (80 ml), and then the reaction product was extracted with ethyl acetate, washed with saturated brine and dried with anhydrous sodium sulfate. Then the solvent was evaporated under a reduced pressure. The thus obtained residue was dissolved in a mixed solvent of 1,4-dioxane (20 ml) and water (10 ml). The resulting solution was mixed with sodium periodate (2.6 g, 12 mmol) and stirred for 2.5 hours as such. Water (100 ml) was added to the reaction solution, and the reaction product was extracted with ethyl acetate, washed with saturated brine and dried with anhydrous sodium sulfate. By evaporating the solvent from the resulting extract under a reduced pressure, 1.3 g of the title compound was obtained (5.3 mmol, 100% in yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355642B1
Source datasetuspto-grants-2002_03
ORD IDord-e5359a06d35040dfa41786a25ad48cb9
Source noteuspto-grants-2002_03