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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170943Generated: October 30, 2026

Hydrogen Peroxide → HCID 59553540, compound

https://huagongshe.com/reaction/1170943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantPotassium CarbonateHCID 11430—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 68765446HCID 68765446—
ReactantHCID 69040547HCID 69040547—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Catalystzinc(II)iodideHCID 9883512—
SolventAcetic AcidHCID 176—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59553540HCID 59553540—

Reaction Steps

To a solution of rac 1-(3,4-dimethoxy-phenyl)-3-(4-trifluoromethyl-phenyl)-propylamine (accessed according to the procedure described for example 126 and 127, step 2 from 2-methyl-propane-2-sulfinic acid [1-(3,4-dimethoxy-phenyl)-3-(4-trifluoromethyl-phenyl)-propyl]-amide, 213 mg, 0.63 mmol) in THF (2 mL) was added 3-pyridinecarboxaldehyde (71 μl, 0.75 mmol), trimethylsilyl cyanide (118 μl, 0.94 mmol) and a catalytic amount of zinc iodide. The solution was stirred for 3 h at ambient temperature before it was diluted with DMSO (0.5 mL) and potassium carbonate (35 mg, 0.25 mmol) and hydrogen peroxide (35% in water, 82 μl, 0.94 mmol) were added. After stirring for 18 h at ambient temperature further hydrogen peroxide (35% in water, 41 μl, 0.47 mmol) was added and stirring continued for 3 h. It was diluted with methanol (0.5 mL) and palladium on charcoal 10% (5 mg) and acetic acid (50 μl) were added. Under an hydrogen atmosphere of hydrogen the reaction mixture was stirred for 3 h at ambient temperature. Sodium borohydride (50 mg) was added and the stirring was continued for 1 h. Purification by chromatography (SiO2, heptane:(ethyl acetate:triethylamine=95:5)=50:50 to 0:100) afforded the title compound as a racemic mixture (1:1) of diastereomers (127 mg, 43%) as a white solid. MS m/e: 472.5 [M−H]−

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829563B2
Source datasetuspto-grants-2010_11
ORD IDord-1e816d11c31f4cfa9df8c09e8f60911c
Source noteuspto-grants-2010_11