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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260936Generated: October 30, 2026

Peracetic Acid → 34748-97-5

https://huagongshe.com/reaction/2260936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPeracetic AcidHCID 6585—
ReactantSodium AcetateHCID 517045—
Reactant1,9-CyclohexadecadieneHCID 534870—
Reactant(1E,9E)-cyclohexadeca-1,9-dieneHCID 5362807—
Reactant1,9-Cyclohexadecadiene, (E,Z)-HCID 6033060—
Reactant17-Oxabicyclo[14.1.0]heptadec-8-eneHCID 19838536—
Reactant4277-06-9HCID 44148196—
Reactant34748-97-5HCID 56841879—
SolventDichloromethaneHCID 6344—
Product34748-97-5HCID 54230859—

Reaction Conditions

Temperature0 °C

Reaction Steps

10 g 1,9-cyclohexadecadiene of the following composition are added to a solution of 14.1 g sodium acetate in 75 ml methylene chloride and the mixture is cooled to 0° C.: (Z,Z)-1,9-cyclohexadecadiene 18%, (E,Z)-1,9-cyclohexadecadiene 54%, (E,E)-1,9-cyclohexadecadiene 28%. 8.6 g peracetic acid (40% strength) in 15 ml methylene chloride are slowly added dropwise at this temperature and the mixture is subsequently stirred for three hours at 0° C. The reaction solution is poured on to ice-water and extracted once with methylene chloride. The combined organic phases are washed with saturated NaCl solution and subsequently dried with magnesium sulfate, and after removal of the solvent 9.0 g of crude product are obtained. After purification by chromatography with ethyl acetate/cyclohexane, a product having the following composition is obtained: (E)-17-oxabicyclo[14.1.0]heptadec-8-ene (1) 33%, (E)-17-oxabicyclo[14.1.0]heptadec-8-ene (2) 28%, (Z)-17-oxabicyclo[14.1.0]heptadec-8-ene (3) 21%, (Z)-17-oxabicyclo[14.1.0]heptadec-8-ene (4) 18%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846886B2
Source datasetuspto-grants-2010_12
ORD IDord-3ea3f627ac084da6bafffe4eb0b664e5
Source noteuspto-grants-2010_12