HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentanone → Cyclopentanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 1-Amino-3,3,5-trimethylcyclohexyl hydroperoxide | HCID 21510183 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Cyclopentanone | HCID 8452 | — |
| Product | 3,3,5-Trimethylcyclohexanone | HCID 13398 | — |
Reaction Steps
To a stirred mixture of cyclopentanone (33.8 g.) and ethanol (100 c.c.) containing ammonium acetate (3.2 g.) and kept at or below 0°C, was added 1-amino-3,3,5-trimethylcyclohexyl hydroperoxide (44.6 g., 68% pure). After storing at 0°C overnight the reaction mixture was worked up as in the previous Examples to give unreacted cyclopentanone and dihydroisophorone together with a fraction (20.0 g.) b.p. 82° - 86°/0.5 mm.Hg. This last fraction was redistilled to give: material b.p. 74° - 76°C/0.3 mm.Hg., peroxide equivalent 202, shown by mass spectroscopy to be a mixture of the peroxide ##SPC61##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03983142 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-1101c6c786f842a7aae9a39ff356208b |
| Source note | uspto-grants-1976_09 |