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 | 85% |
Reaction Steps
After charging 100 parts of α-bromo-γ-butyrolactone and 104.4 parts of methacrylic acid (2.0 times in mole based on α-bromo-γ-butyrolactone), a three times amount of methyl isobutyl ketone based on α-bromo-γ-butyrolactone was added thereto to form a solution. To this solution was added dropwise 183.6 parts of triethylamine (3.0 times in mole based on α-bromo-γ-butyrolactone) Then, the solution was stirred at room temperature for about 10 hours. After filtration, the organic layer was washed with 5% aqueous sodium hydrogen carbonate solution and then washed twice with water. The organic layer was concentrated to give α-methacryloyloxy-γ-butyrolactone represented by the following formula in 85% yield:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06548221B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-b73dcd9deec6400a8df3e2f05396cb60 |
| Source note | uspto-grants-2003_04 |