HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methacrylic Acid → gamma-Butyrolactone methacrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methacrylic Acid | HCID 4093 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2(3H)-Furanone, 3-bromodihydro- | HCID 95463 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | gamma-Butyrolactone methacrylate | HCID 11206014 | 85% |
Reaction Steps
100 g of α-bromo-γ-butyrolactone and 104.4 g of methacrylic acid (2.0 mole times with respect to α-bromo-γ-butyrolactone) were charged, and methyl isobutyl ketone was added thereto in an amount of 3 weight times that of α-bromo-γ-butyrolactone to prepare a solution. Then, 183.6 g of triethylamine (3.0 mole times with respect to α-bromo-γ-butyrolactone) was added dropwise thereto, followed by stirring at room temperature for about 10 hours. After filtration, an organic layer was washed with 5% by weight aqueous solution of sodium bicarbonate, followed by washing with water for 2 times. The organic layer was concentrated to obtain α-methacryloyloxy-γ-butyrolactone represented by the following formula in a 85% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06239231B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-5b8e4dd6c58e47f68aa2394d46d03b36 |
| Source note | uspto-grants-2001_05 |