HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345615Generated: October 28, 2026
Water → 2-Phenoxy-2-trifluoromethyl-1,3-dioxolane
https://huagongshe.com/reaction/345615
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloroethyl trifluoroacetate | HCID 12574717 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Phenoxy-2-trifluoromethyl-1,3-dioxolane | HCID 14401448 | 47.1% |
Reaction Steps
A solution of 23.5 g (0.25 mol) of phenol in 50 mL of DMSO was added dropwise to a stirred suspension of 12.0 g (0.25 mol) of 50% NaH in mineral oil in 100 mL of DMSO maintained at 15°-20° by cooling. After evolution of gas had slowed, cooling and stirring were continued while 44.3 g (0.25 mol) of 2-chloroethyl trifluoroacetate were added. The temperature of the reaction mixture was kept below 30° while the exotherm which occurred subsided, then the resulting mixture was stirred overnight, poured into 1 L of water, and extracted with 200 mL, then two 100 mL portions, of ether. The resulting ether solutions were washed with water, dried over CaSO4, and distilled to give 27.6 g (47% yield) of 2-phenoxy-2-trifluoromethyl-1,3-dioxolane, b.p. 52°-54° at 80 Pa (0.6 mm). IR (neat) and NMR (CCl4) spectra were consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05057586 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-19fc4bae674e49d1aec0fc942d8ef00c |
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| Source note | uspto-grants-1991_10 |
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