HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 1-Methyl-4-oxo-5-pentylcyclopent-2-en-1-yl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 13137234 | HCID 13137234 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-Methyl-4-oxo-5-pentylcyclopent-2-en-1-yl acetate | HCID 13517255 | — |
Reaction Steps
Into the same flask as used in Example 1, dl-3-hydroxy-2-n-pentyl-3-methyl-4-cyclopentenone (18.2 g), triethylamine (0.1 g) and acetic anhydride (36 g) were charged, and the resultant mixture was stirred at 60°-80° C. for 3 hours. After completion of the reaction, the reaction mixture was subjected to the same work-up as in Example 1 to give 21.9 g of dl-3-acetoxy-2-n-pentyl-3-methyl-4-cyclopentenone. Yield, 98%. B.P., 100°-110° C./0.1-0.3 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04729953 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-9f45e4b61f8c422593f1fc787c080016 |
| Source note | uspto-grants-1988_03 |