HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxygen → Dimethyl 2-octylmalonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | 1-Octene | HCID 8125 | — |
| Reactant | HCID 18551911 | HCID 18551911 | — |
| Catalyst | Cobalt diacetate | HCID 6277 | — |
| Catalyst | Manganous Acetate | HCID 12525 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 11728009 | HCID 11728009 | 5% |
| Product | Dimethyl 2-octylmalonate | HCID 14745592 | 56% |
| Product | HCID 18551906 | HCID 18551906 | 6% |
Reaction Steps
A mixture of 30 mmol of dimethyl malonate, 2 mmol of 1-octene, 0.04 mmol of manganese(II) acetate, 0.01 mmol of cobalt(II) acetate and 2 ml of acetic acid was stirred at 90° C. in an atmosphere of a gaseous mixture of nitrogen and oxygen (9:1) (1 atm=0.101 MPa) for 3 hours. The resulting reaction mixture was analyzed to find that dimethyl 2-octylmalonate (yield: 56%), dimethyl 2-(2-oxooctyl)malonate (trace amount), α-methoxycarbonyl-γ-hexyl-γ-butyrolactone (yield: 6%), dimethyl 2-(2-octyloctyl)malonate (yield: 5%) and dimethyl 2,2-dioctylmalonate (yield: 3%) were produced with a conversion from 1-octene of 96%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06548713B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-62ed7d7c0e81408e9ae4f688a292a181 |
| Source note | uspto-grants-2003_04 |