HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193584Generated: November 1, 2026
Phenol → 2-Trifluoromethyl-2-(2-phenoxytetrafluoroethyl)-1,3-dioxolane
https://huagongshe.com/reaction/1193584
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenol | HCID 996 | — |
| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloroethyl trifluoroacetate | HCID 12574717 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | 2-Trifluoromethyl-2-(2-phenoxytetrafluoroethyl)-1,3-dioxolane | HCID 14401449 | 73.3% |
Reaction Steps
A suspension of 12.0 g (0.25 mol) of 50% NaH in mineral oil in 100 mL of dry diglyme (diethylene glycol dimethyl ether) was stirred at 25° under nitrogen while a solution of 23.5 g (0.25 mol) of phenol in 50 mL of diglyme was added. The resulting mixture was stirred until evolution of gas ceased, then charged into a 400 mL metal tube along with 44.3 g (0.25 mol) of 2-chloroethyl trifluoroacetate and 40 g (0.70 mol) of tetrafluoroethylene. The resulting mixture was agitated for 6 h while the temperature rose to 34° and subsided. Next the mixture was heated at 50° for 6 h. The resulting reaction mixture was added to 1 L of water, thereby causing the formation of layers. The lower layer was separated, washed with water, dried over CaSO4, and distilled to give 61.2 g (73% yield) of 2-trifluoromethyl-2-(2-phenoxytetrafluoroethyl)-1,3-dioxolane, b.p. 64°-67° at 13 Pa (0.1 mm). The IR (CCl4) and NMR (CCl4) spectra of the product were consistent with the structure assignment.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04810806 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-8292f1c3ea634cffb1dd1b96909900c6 |
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| Source note | uspto-grants-1989_03 |
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