Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 1,9-Cyclohexadecadiene | HCID 534870 | — |
| Reactant | (1E,9E)-cyclohexadeca-1,9-diene | HCID 5362807 | — |
| Reactant | 1,9-Cyclohexadecadiene, (E,Z)- | HCID 6033060 | — |
| Reactant | 17-Oxabicyclo[14.1.0]heptadec-8-ene | HCID 19838536 | — |
| Reactant | 4277-06-9 | HCID 44148196 | — |
| Reactant | 34748-97-5 | HCID 56841879 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 34748-97-5 | HCID 54230859 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07846886B2 |
|---|
| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-3ea3f627ac084da6bafffe4eb0b664e5 |
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| Source note | uspto-grants-2010_12 |
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