HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclododecanone → Cyclopentadecanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclododecanone | HCID 13246 | — |
| Reactant | 4-Oxo-pentadecanedioic acid | HCID 20358597 | — |
| Product | Cyclopentadecanone | HCID 10409 | — |
| Product | Cyclododecanone | HCID 13246 | — |
Reaction Steps
4-oxo-pentadecanedioic acid IV is obtainable at the yield of 66.2% based on the moles of cyclododecanone through the referential examples 1 and 2 and Example 1 as mentioned later. Alternatively, the compound IV is obtainable at the yield of 60.8% based on the moles of cyclododecanone through Examples 5 and 7. Further combined with the Referential Example 3, the overall yields of cyclopentadecanone from cyclododecanone are 39.7% and 36.4%, respectively. This fact shows that this invention provides increased yield as another improved advantage in addition to the before-mentioned advantage of avoiding employment of polyphosphoric acid for conversion to ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04085274 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-ee0def43c6dd418581c6e0752d1e001c |
| Source note | uspto-grants-1978_04 |