HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876064Generated: October 30, 2026
Trifluoroacetic acid → HCID 67472847, compound
https://huagongshe.com/reaction/876064
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| Reactant | 1-Fluoro-4-hydroxy-9H-thioxanthen-9-one | HCID 13615013 | — |
| Reactant | 2-Propenoic acid, 2-(2-(ethenyloxy)ethoxy)ethyl ester | HCID 23067259 | — |
| Product | HCID 67472847 | HCID 67472847 | — |
Reaction Steps
1-fluoro-4-hydroxy-thioxanthen-9-one (2.5 g, 0.01 mol), 2,6-di-tert-butyl-4-methylphenol (0.07 g, 0.32 mmol) and trifluoroacetic acid (0.1 g=92.4 μL, 1.2 mmol) were added to 2-(2′-vinyloxyethoxy)ethylacrylate (27.6 g). The mixture was heated to 70° C. and stirred for 4 hours. After cooling down to room temperature, activated Lewatit M600 MB (10 g) was added and stirred for 1 hour. After filtration, a 15 w % solution of acrylic acid 2-{2-[1-(1-fluoro-9-oxo-9H-thioxanthen-4-yloxy)-ethoxy]-ethoxy}-ethyl ester in 2-(2′-vinyloxyethoxy)ethylacrylate was obtained, which was directly used in the radiation curable compositions according to a preferred embodiment of the present invention.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08985753B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-51b3693187f14a5c93cde5cf5e8398a5 |
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| Source note | uspto-grants-2015_03 |
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