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

HRID 1193583Notes

Reaction equation

HRID 1193583 reaction equation
[C:1]1([OH:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[Na+].[F:10][C:11]([F:19])([F:18])[C:12]([O:14][CH2:15][CH2:16]Cl)=[O:13].O>CS(C)=O>[O:7]([C:12]1([C:11]([F:19])([F:18])[F:10])[O:14][CH2:15][CH2:16][O:13]1)[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

6

Procedure

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.

Workup

  1. temperaturemaintained at 15°-20°
  2. temperatureby cooling
  3. temperaturecooling
  4. additionwere added
  5. customwas kept below 30° while the exotherm which
  6. stirringthe resulting mixture was stirred overnight
  7. extractionextracted with 200 mL
  8. washThe resulting ether solutions were washed with water
  9. dry with materialdried over CaSO4
  10. distillationdistilled

Sources & evidence

ORD record
ord-57c0833ed23c4709b7ef10c0d8aa6a13
Source dataset
uspto-grants-1989_03
Patent number
US04810806

Reaction notes

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