HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Oxalate → HCID 86734794, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | HCID 10034704 | HCID 10034704 | — |
| Reactant | HCID 21432375 | HCID 21432375 | — |
| Reactant | HCID 21432376 | HCID 21432376 | — |
| Reactant | HCID 23261195 | HCID 23261195 | — |
| Reactant | HCID 68120576 | HCID 68120576 | — |
| Reactant | HCID 86734795 | HCID 86734795 | — |
| Product | HCID 86734794 | HCID 86734794 | — |
Reaction Steps
In a process for the synthesis of 2-(6-carbomethoxy-cis-hexenyl)-cyclopentane-1,3,4-trione by stepwise converting 2-methyl-2-(3-butynyl)-1,3-dioxolane to 9-oxo-5-decynoic acid, esterifying that acid to methyl 9-oxo-5-decynoate, reducing the latter to 9-oxo-cis-5-decenoate, condensing the methyl 9-oxo-cis-5-decenoate with diethyl oxalate to obtain 2-(6-carbomethoxy-cis-2-hexenyl)-5-ethoxalyl-cyclopentane-1,3,4-trione as an intermediate, and hydrolyzing the intermediate to obtain 2-(6-carbomethoxy-cis-hexenyl)-cyclopentane-1,3,4-trione, the improvement which comprises:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04026911 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-b1680ff5d95b4658a3f43471413f72cd |
| Source note | uspto-grants-1977_05 |