HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526802Generated: October 30, 2026
Boron trifluoride → HCID 21954468, compound
https://huagongshe.com/reaction/526802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | 4-Methoxyphenol | HCID 9015 | — |
| Reactant | HCID 72550680 | HCID 72550680 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21954468 | HCID 21954468 | — |
Reaction Steps
In a 50 mL four-necked flask, 0.5 g of α,α,β-trimethyl-β-methacryloyloxymethyl-β-propiolactone was put, and dissolved in 10 g of ethyl acetate, and a stirrer, a thermometer and a Dimroth cooling tube were connected thereto. Further, 5 mol % of diethyl ether complex of boron trifluoride was added thereto based on the substrate, and 5 mg of p-methoxyphenol was added thereto, and while solution temperature was kept at 30° C., the resulting mixture was stirred. After the mixture was stirred for 2 hours, the resulting reaction mixture was washed with a 10% sodium carbonate aqueous solution and saturated brine, and dried over magnesium sulfate. After separation by filtration, the solvent was distilled off using an evaporator. A quantitative isomerization reaction to crude α,α,β-trimethyl-β-methacryloyloxy-γ-butyrolactone represented by formula (9) was confirmed. FIG. 2 shows an NMR measurement chart.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346775B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-47a302d6d84b4fa98475e536215d3f4c |
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| Source note | uspto-grants-2016_05 |
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