HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20306565, compound → HCID 70583183, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20306565 | HCID 20306565 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Lindlars catalyst | HCID 131709914 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 70583183 | HCID 70583183 | — |
Reaction Steps
A 4.5 g quantity of 5-methoxycarbonyl-4-methoxycarbonylmethyl-5-(2-pentynyl)-2-cyclopentenone (compound (2-a)) is dissolved in a mixture of 50 ml of n-hexhane and 50 ml of acetone, and 7 g of a Lindlar catalyst is added to the solution. Hydrogen gas is introduced into the solution with stirring. The reaction is completed when the solution has absorbed the theoretical amount of the gas. On completion of the reaction, the catalyst is filtered off from the reaction mixture, and the filtrate is concentrated at reduced pressure. The residue is distilled in a vacuum, affording 5-methoxycarbonyl-4-methoxycarbonylmethyl-5-(cis-2-pentenyl)-2-cyclopentenone (compound (2-b), R1 =CH3, R2 =CH3) in a yield of 99.8%, b.p. 81-85° C./0.005 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04173707 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-3218e550aebf47e1ace4a1766f6492c6 |
| Source note | uspto-grants-1979_11 |