HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalic Acid → Hedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | 2-Pentylidenecyclopentanone | HCID 86000 | — |
| Reactant | Cyclopentanone, 2-(1-hydroxypentyl)- | HCID 162060 | — |
| Product | Hedione | HCID 102861 | — |
Reaction Steps
The reaction in Comparative Example 1 was carried out 3 times, the product was distilled to recover cyclopentanone and water, then 0.0206 mol oxalic acid was added to 1.11 mol 2-(1-hydroxy-n-pentyl)cyclopentanone and 0.012 mol 2-pentylidene cyclopentanone from the product, and the mixture was reacted at 120° C. Thereafter, the reaction was carried out in the same manner as in Example 7, to give methyl 3-oxo-2-pentylcyclopentylacetate. As a result, the yield in the whole process was 28%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07161041B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-b92483900ede46188e7a2cbdc6390ddd |
| Source note | uspto-grants-2007_01 |