HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370325Generated: October 31, 2026
m-Chloroperbenzoic acid → (+/-)-7-(2'-Acetoxyethyl)-2-oxepanone
https://huagongshe.com/reaction/370325
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(2'-Acetoxyethyl) cyclohexanone | HCID 11126942 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (+/-)-7-(2'-Acetoxyethyl)-2-oxepanone | HCID 23283899 | — |
Reaction Steps
Under an argon atmosphere, sodium bicarbonate (1.78 g, 21.20 mmol) and 80-90% w/w MCPBA (4.95 g, 28.26 mmol) were added to a solution of (±)-2-(2'-acetoxyethyl)cyclohexanone (2.60 g, 14.13 mmol) (0.50 mmol) in dichloromethane (70 ml) at room temperature. The mixture was stirred at room temperature for 3 h, and diluted with dichloromethane (80 ml) and washed sequentially with a saturated sodium sulphite solution (3×100 ml), distilled water (100 ml) and brine (100 ml). The organic phase was dried over magnesium sulphate. After filtration, the solvent was evaporated under reduced pressure to give the crude product which was purified by flash column chromatography using hexane-ethyl acetate (2:3) as eluent to give (±)-7-(2'-acetoxyethyl)-2-oxepanone, as a colourless oil (2.76 g, 98% yield). Rf 0.40 (hexane-ethyl acetate, 7:3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06140512 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-a22791c55d7144289f59ea0e3740ed9c |
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| Source note | uspto-grants-2000_10 |
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