HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxygen → 2-Hydroxy4,4-dimethyl-gamma-butyrolactone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Ethyl 2,4-dihydroxy-4-methylpentanoate | HCID 11378808 | — |
| Catalyst | Cobalt diacetate | HCID 6277 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Hydroxy4,4-dimethyl-gamma-butyrolactone | HCID 10197703 | — |
Reaction Steps
A mixture of 3 mmol of ethyl acrylate, 3 ml of 2-propanol, 0.6 mmol of N-hydroxyphthalimide, 0.003 mmol of cobalt(II) acetate, 0.015 mmol of acetylacetonatocobalt(III), and 1 ml of acetonitrile was stirred at 60° C. in an oxygen atmosphere (1 atm) for 12 hours. A gas chromatographic analysis of products in a reaction mixture revealed that ethyl 2,4-dihydroxy-4-methylpentanoate and α-hydroxy-γ,γ-dimethyl-γ-butyrolactone were formed in yields of 1.5% and 75%, respectively, with a conversion from ethyl acrylate of 81%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07183423B1 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-18d516d3031f4293a26a4586fe747ca1 |
| Source note | uspto-grants-2007_02 |