HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 2-(2-Phenoxytetrafluoro-ethyl)-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloroethyl formate | HCID 246748 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | 2-(2-Phenoxytetrafluoro-ethyl)-1,3-dioxolane | HCID 14401450 | 57% |
Reaction Steps
A suspension of 17.3 g (0.36 mol) of 50% NaH in mineral oil in 100 mL of diglyme was treated with a solution of 33.9 g (0.36 mol) of phenol in 50 mL of diglyme. The resulting mixture was stirred overnight and then charged into a 400 mL metal tube along with 38.6 g (0.36 mol) of 2-chloroethyl formate and 40 g (0.40 mol) of tetrafluoroethylene. The resulting mixture was agitated for 12 h, and then added to 1 L of cold water, thereby causing the formation of layers. The lower layer was washed with water, dried over CaSO4, and distilled to afford 54.5 g (57% yield) of 2-(2-phenoxytetrafluoro-ethyl)-1,3-dioxolane, b.p. 62°-65° at 8 Pa (0.06 mm). The IR (neat) and NMR (CCl4) spectra of the product were consistent with the assigned sstructure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04810806 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-e697018045234cdc881d036f3e49c016 |
| Source note | uspto-grants-1989_03 |