Hydrogen Peroxide → Suberic acid

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.

1. additionTo a mixture of [Mn2O3(Me3-TACN)2] (PF6)2
2. stirringthe mixture was stirred for additional 15 hours
3. customThe organic layer was separated
4. washthe aqueous layer was washed with Et2O (3×15 ml)
5. extractionwas extracted with Et2O (3×20 ml)
6. dry with materialThe combined organic extracts were dried over anhydrous Na2SO4
7. customThe solvents were removed in vacuo

ORD record

ord-296afa8d2b3c4837964447fd491e585c

Source dataset

uspto-grants-2015_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08946470B2