HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → 2,3-Epoxy-4-(2-tetrahydropyranyloxy)cyclopentan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(Tetrahydro-pyran-2-yloxy)-cyclopent-2-enone | HCID 12838010 | — |
| Reactant | 4-t-Butyldimethylsiloxy-2-n-octylthiocyclopent-2-en-1-one | HCID 20380374 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,3-Epoxy-4-(2-tetrahydropyranyloxy)cyclopentan-1-one | HCID 20380347 | 84% |
Reaction Steps
One gram of 4-(2-tetrahydropyranyloxy)cyclopent-2-en-1-one was dissolved in 20 ml of methanol, and 10 ml of 30% hydrogen peroxide was added at room temperature. Then, with ice cooling, 3 ml of a 2 N aqueous solution of sodium hydroxide was added slowly. The mixture was stirred at room temperature for 1.5 hours. The reaction mixture was post-treated in the same way as in Example 1, (1). The resulting crude product was chromatographed on a thin layer plate with cyclohexane/ethyl acetate (=7/3) to afford 730 mg of 2,3-epoxy-4-(2-tetrahydropyranyloxy)cyclopentan-1-one in a yield of 84%. The product had the following spectral data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04180672 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-5f425e3822f0430cbb3da60d10d1f887 |
| Source note | uspto-grants-1979_12 |