HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372122Generated: October 30, 2026
Hydrogen Peroxide → HCID 20354850, compound
https://huagongshe.com/reaction/372122
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20354852 | HCID 20354852 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 20354850 | HCID 20354850 | — |
Reaction Steps
A stirred solution of 2-(3-acetoxyoctyl)cyclopent-2-enone (31.8 g.) [prepared as described in (f) above] in methanol (700 ml.) was treated slowly with aqueous hydrogen peroxide solution (45 ml. of "100 vol." solution) and aqueous 4N sodium hydroxide solution (15 ml.) at 5° to 10° C. and allowed to stand at room temperature for 18 hours. The solution was concentrated in vacuo (to about 100 ml. volume), and water (100 ml.) was added to the residue. The mixture was extracted with chloroform and the chloroform extract was washed with water and dried over magnesium sulphate. The solvent was removed in vacuo to give 2-(3-acetoxyoctyl)-2,3-epoxycyclopentanone (26.4 g.) which was used as starting material in the following preparation (h) of 5-acetoxy-2-(3-acetoxyoctyl)cyclopent-2-enone without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04088821 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-6ee7b2341032409fbb294ac5c677e50d |
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| Source note | uspto-grants-1978_05 |
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