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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585380Generated: October 30, 2026

Hydrogen Peroxide → HCID 11077506, compound

https://huagongshe.com/reaction/1585380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantIodineHCID 807—
ReactantOxygenHCID 977—
ReactantMethylene blue cationHCID 4139—
ReactantDivinyl sulfideHCID 12321—
Reactant1,2-DioxetaneHCID 122029—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 86754405HCID 86754405—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 11077506HCID 11077506—

Reaction Steps

The vinyl sulfide of Example 1(b) (0.113 g) was irradiated for 15 min in 20 mL of methanol containing a few crystals (<1 mg) of methylene blue with continuous oxygen bubbling at -78° C. using a 1000 W Na lamp. Iodine (0.096 g) and 1 mL of 30% H2O2 were added and the mixture warmed to room temperature. Progress of the reaction was monitored by the disappearance of starting material by TLC (20% ethyl acetate in hexane) and the appearance of new bands which emitted blue light when the plate was heated and by observing the color of chemiluminescence from an aliquot of the reaction solution reacted with 0.1 M TBAF in DMSO. The yellow emission of dioxetane 1 was gradually replaced by the blue emission of dioxetane 6 over a period of several hours. The solution was concentrated to 1-2 mL and separated on preparative TLC with 10% ethyl acetate in hexane. The band containing dioxetane 6 was collected, desorbed and evaporated yielding 77 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05936101
Source datasetuspto-grants-1999_08
ORD IDord-c3c8ed172dc54fa0adee247fe312c514
Source noteuspto-grants-1999_08