Ethylene Glycol → HCID 19047161, compound

HRID 275447Notes

Reaction equation

HRID 275447 reaction equation
[Cl:1][C:2]1[C:7]([CH:8]=[O:9])=[CH:6][C:5]([N:10]2[C:15](=[O:16])[CH2:14][CH:13]([C:17]([F:20])([F:19])[F:18])[CH2:12][C:11]2=[O:21])=[C:4]([F:22])[CH:3]=1.[CH2:23]([OH:26])[CH2:24]O.O.[C:28]1(C)C=CC(S(O)(=O)=O)=CC=1.O>C1(C)C=CC=CC=1>[Cl:1][C:2]1[C:7]([CH:8]2[O:26][CH2:23][CH2:24][CH2:28][O:9]2)=[CH:6][C:5]([N:10]2[C:11](=[O:21])[CH2:12][CH:13]([C:17]([F:19])([F:18])[F:20])[CH2:14][C:15]2=[O:16])=[C:4]([F:22])[CH:3]=1

Participants

6

Procedure

To 3.4 g (.10 mmol) N-(4'-chloro-2'-fluoro-5'-formylphenyl)-3-(trifluoromethyl)glutarimide (Compound 94) in 110 ml toluene was added 0.94 g (15 mmol) ethylene glycol and a catalytic amount of p-toluenesulfonic acid monohydrate (0.48 g, 2 mmol). The mixture was refluxed for 72 h with removal of water via a Dean-Stark trap. The solvent was removed in vacuo and the residue was partitioned between EtOAc and water. The organics were washed with water and brine, dried over MgSO4, then filtered and concentrated to leave 4.1 g (105 % yield) of an oily taffy containing mostly product by NMR analysis. Recrystallization from Et2O afforded 1.0 g of the 1,3-dioxane as a pale yellow solid, m.p. 158°-161° C.

Workup

  1. customThe solvent was removed in vacuo
  2. customthe residue was partitioned between EtOAc and water
  3. washThe organics were washed with water and brine
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto leave 4.1 g (105 % yield) of an oily taffy
  8. additioncontaining mostly product by NMR analysis
  9. customRecrystallization from Et2O

Sources & evidence

ORD record
ord-cced3c8d4135437f959b530a3fe2aa69
Source dataset
uspto-grants-1995_02
Patent number
US05393735

Reaction notes

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