Hydrogen Peroxide → 1,2-Epoxycyclooctane
Reaction equation
[CH:1]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH:2]=1.[OH:9]O>>[O:9]1[CH:2]2[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH:1]12Participants
3
Procedure
The solid mixed phase after extraction in Example 1 was dried under reduced pressure for about 12 hours. 0.110 g (1.00 mmol) of cyclooctene was added to the solid mixed phase after drying under reduced pressure, and stirred well. Further, 0.10 mL (0.90 mmol) of 31% aqueous hydrogen peroxide was added and stirred well. Then, the mixture was allowed to stand still at 25° C. for 24 hours. Thereafter, a colorless solid of epoxycyclooctane was obtained in the same manner as in Example 1. The epoxide yield was 83%.
Workup
- additionThe solid mixed phase
- extractionafter extraction in Example 1
- customwas dried under reduced pressure for about 12 hours
- additionmixed phase
- customafter drying under reduced pressure
- stirringstirred well
Sources & evidence
- ORD record
- ord-5253119718c3423894984dfe29d12cf8
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08334394B2
Reaction notes
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