HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methacrylic Acid → gamma-Butyrolactone methacrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methacrylic Acid | HCID 4093 | — |
| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Reactant | 2(3H)-Furanone, 3-bromodihydro- | HCID 95463 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | gamma-Butyrolactone methacrylate | HCID 11206014 | — |
Reaction Steps
A vessel was charged with 100 g of α-bromo-γ-butyrolactone and 104.4 g of methacrylic acid(2.0 times the molar amount of a-bromo-γ-butyrolactone). Then. methyl isobutyl ketone in a weight three times the weight of α-bromo-γ-butyrolactone was added thereto to form a solution. To the solution was added dropwise 183.6 g of triethylamine(3.0 times the molar amount of α-bromo-γ-butyrolactone), followed by stirring for about 10 hours at room temperature. After filtration, the resulting organic layer was washed with an aqueous solution of 5 wt % sodium bicarbonate and then washed with water twice. The organic layer was concentrated to obtain α-methacryloyloxy-γ-butyrolactone represented by the following formula.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06495306B2 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-3f067603692b48cb8ab9c104a4820c8e |
| Source note | uspto-grants-2002_12 |