HuagongsheHuagongshe Chemistry Print Report · For research reference only
Heptafluorobutyric acid → (3,4,4-Trifluoro-3-butenyl) heptafluorobutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Heptafluorobutyric acid | HCID 9777 | — |
| Reactant | 4-Bromo-1,1,2-trifluorobut-1-ene | HCID 66333 | — |
| Catalyst | Silver | HCID 23954 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (3,4,4-Trifluoro-3-butenyl) heptafluorobutyrate | HCID 53853464 | — |
Reaction Steps
To a stirred mixture of 3.2 grams (0.01 mole) of the silver salt of heptafluorobutyric acid in 40 ml of diethyl ether was added dropwise 1.9 grams (0.01 mole) of 4-bromo-1,1,2-trifluoro-1-butene in 10 ml of diethyl ether. Upon completion of addition the reaction mixture was stirred for two hours at ambient temperature, then was heated under reflux for one hour. The ether solvent was removed by distillation and the residual oil distilled under reduced pressure to give 1.0 gram of (3,4,4-trifluoro-3-butenyl) heptafluorobutyrate; b.p. 25° C./4.0 mm Hg. The nmr spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04952580 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-2edf9e5c93d1426b808fda045fe414fd |
| Source note | uspto-grants-1990_08 |