HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2H-Perfluoroisopropyl 2-fluoroacrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1,1,3,3,3-Hexafluoro-2-propanol | HCID 13529 | — |
| Reactant | 2-Fluoroacryloyl chloride | HCID 2783335 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2H-Perfluoroisopropyl 2-fluoroacrylate | HCID 2778359 | — |
Reaction Steps
12 g of 2-fluoroacryloyl chloride and 27 g of 1,1,1,3,3,3-hexafluoro-2-propanol were introduced into a round-bottomed flask placed in an ice bath. 16 g of triethylamine were added portionwise to the reaction mixture. After reacting for an additional 3 h, approximately 70 ml of water were added. The aqueous and organic phases were subsequently separated and the organic phase was analysed by GC. The conversion of the 1,1,1,3,3,3-hexafluoroisopropanol was 68%. The yield of ester, based on the amount of 2-fluoroacrylic acid employed in the first stage, was 66%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07304191B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-c02449b42c1f45c4ba80c9b51c107c04 |
| Source note | uspto-grants-2007_12 |