HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trichloroethanol → 2,2,2-Trichloroethyl-2-fluoroacrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trichloroethanol | HCID 8259 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Fluoroacryloyl chloride | HCID 2783335 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,2,2-Trichloroethyl-2-fluoroacrylate | HCID 2782530 | — |
Reaction Steps
12 g of 2-fluoroacryloyl chloride and 26 g of 2,2,2-trichloroethanol were introduced into a round-bottomed flask placed in an ice bath. 17 g of triethylamine were added portionwise to the reaction mixture. After reacting for an additional 3 h, approximately 50 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 2,2,2-trichloroethanol was 52%. The yield of ester, based on the amount of 2-fluoroacrylic acid employed in the first stage, was 67%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07304191B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-d4d39609322f436bbc68b8ba4785752a |
| Source note | uspto-grants-2007_12 |