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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483890Generated: October 30, 2026

Water → 2-Phenoxy-2-trifluoromethyl-1,3-dioxolane

https://huagongshe.com/reaction/483890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenolHCID 996—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloroethyl trifluoroacetateHCID 12574717—
SolventDimethyl SulfoxideHCID 679—
Product2-Phenoxy-2-trifluoromethyl-1,3-dioxolaneHCID 1440144847.1%

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. Anal.: Calcd for C10H9F3O3 : C, 51.29; H, 3.87; F, 24.34. Found: C, 51.19; H, 3.92; F, 24.49.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05227500
Source datasetuspto-grants-1993_07
ORD IDord-b7ed815ab0894616a0d3ed980f68ddc5
Source noteuspto-grants-1993_07