HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl 7-(4-hydroxycyclopent-2-en-1-on-2-yl)-5-heptynoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-(4-Hydroxycyclopent-2-en-1-on-2-yl)-5-heptynoic acid | HCID 14774425 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 7-(4-hydroxycyclopent-2-en-1-on-2-yl)-5-heptynoate | HCID 14656225 | 81.4% |
Reaction Steps
A stirred mixture of 5.8 g of 7-(4-hydroxycyclopent-2-en-1-on-2-yl)-5-heptynoic acid, 3.95 g of potassium carbonate, 7.4 g of iodomethane and 52 ml of acetone was refluxed for 2.5 hours. Most of the acetone was evaporated and the residue was partitioned with water and ether. The ether layer was separated, washed with brine, dried and concentrated, giving 5.02 g of the desired compound as an oil; PMR δ 3.72 (3H, s, methyl ester).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04958037 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-24863c94644649c4bc1e57ddfd25ad83 |
| Source note | uspto-grants-1990_09 |