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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844759Generated: October 31, 2026

Hydrogen Peroxide → Suberic acid

https://huagongshe.com/reaction/1844759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactant2,6-Dichlorobenzoic acidHCID 5758—
Reactant1-CycloocteneHCID 13609—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventMethyl Ethyl KetoneHCID 6569—
ProductSuberic acidHCID 1045740%

Reaction Steps

To a mixture of [Mn2O3(Me3-TACN)2] (PF6)2.H2O (16.2 mg, 20 μmol, 0.2 mol %) and 2,6-dichlorobenzoic acid (57.3 mg, 0.30 mmol, 3.0 mol %) in 2-butanone (7 ml) was added H2O2 (30 μl of a 50% aq. solution, 0.53 mmol) at room temperature and the resulting mixture was stirred for 20 min. Subsequently cyclooctene (1.149 g, 9.90 mmol) was added together with 2-butanone (2 ml) and water (1 ml). H2O2 (5.67 ml of a 50% aq. solution, 100 mmol, 10.0 equiv.) was then added at 40° C. using a syringe pump (0.7 ml/h). New batches of [Mn2O3(Me3-TACN)2] (PF6)2.H2O (16.2 mg, 20 μmol, 0.2 mol % per batch) were added to the reaction mixture 1.5, 3, 4.5, 6 and 7.5 hours after the addition of H2O2 had commenced. When the addition of H2O2 was completed, the mixture was stirred for additional 15 hours. Water (10 ml) and Et2O (10 ml) were added and the pH of the aqueous layer was set to pH >9 by adding some saturated NaHCO3 (aq.). The organic layer was separated and the aqueous layer was washed with Et2O (3×15 ml). The pH of the aqueous layer was subsequently set to pH <2 with some 10% HCl (aq.) and was extracted with Et2O (3×20 ml). The combined organic extracts were dried over anhydrous Na2SO4. The solvents were removed in vacuo yielding 926 mg of a solid with a purity of circa 74% (determined by 1H NMR), 40% yield of suberic acid. N.B. NMR showed other compounds as well, including 2,6-dichlorobenzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946470B2
Source datasetuspto-grants-2015_02
ORD IDord-296afa8d2b3c4837964447fd491e585c
Source noteuspto-grants-2015_02