Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclooctanone | HCID 10403 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 2-Oxonanone | HCID 138568 | 73.4% |
Reaction Steps
43.5 g (345 mmol) of cyclooctanone (compound of formula (VI) with n=6) (ACROS) are placed in solution in 430 ml of dichloroethane. 170 g (985 mmol) of meta-chloroperbenzoic acid are then added. The medium is heated to 80° C. for 48 hours. At room temperature, 400 ml of a Na2S2O5 and NaHCO3 saturated solution (1/1 v/v) are added. The medium is strongly stirred for 18 hours. The organic phase is separated and placed into the presence of KI and H2O for 6 hours. The organic phase is separated and washed with a Na2S2O3 saturated solution, with a NaCl saturated solution, and is then dried on MgSO4, filtered and concentrated in vacuo in order to obtain 36 g of crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07928254B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-692924524aaf452e94790668f1f41bf8 |
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| Source note | uspto-grants-2011_04 |
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