Ethylene Glycol → 2-(2-Methyl[1,3]dioxolane-2-yl)furan

HRID 865682

Reaction equation

HRID 865682 reaction equation
[C:1]([C:4]1[O:5][CH:6]=[CH:7][CH:8]=1)(=[O:3])[CH3:2].[CH2:9](O)[CH2:10][OH:11].C(OCC)(OCC)OCC.C(OCC)(=O)C>O.C1(C)C=CC(S(O)(=O)=O)=CC=1.O>[CH3:2][C:1]1([C:4]2[O:5][CH:6]=[CH:7][CH:8]=2)[O:11][CH2:10][CH2:9][O:3]1

Participants

7

Procedure

A mixture of 4 mL (139.6 mmol) 2-acetylfuran, 8.7 mL (156 mmol) of ethylene glycol, 198 mg (1 mmol) of p-toluenesulfonic acid monohydrate, and 22 mL (132.3 mmol) of triethyl orthoformate was reacted at room temperature under N2 for 3 days. The reaction mixture was poured into a mixture of ethyl acetate (100 mL) and water (100 mL). The aqueous layer was extracted with ethyl acetate (3×50 mL), and the combined organic layer was washed with water (100 mL), sodium bicarbonate solution (150 mL), and brine (100 mL). The organic layer was dried over MgSO4, concentrated in vacuo, and the residue was distilled under reduced pressure (1.5 torr) to afford 9.98 g (50%) of 2-(2-methyl-1,3-dioxolan-2-yl)-furan, as a clear oil, b.p. 24° C./1.5 mm.

Workup

  1. customwas reacted at room temperature under N2 for 3 days
  2. extractionThe aqueous layer was extracted with ethyl acetate (3×50 mL)
  3. washthe combined organic layer was washed with water (100 mL), sodium bicarbonate solution (150 mL), and brine (100 mL)
  4. dry with materialThe organic layer was dried over MgSO4
  5. concentrationconcentrated in vacuo
  6. distillationthe residue was distilled under reduced pressure (1.5 torr)

Sources & evidence

ORD record
ord-a9e07ebfb8974ade8c66484c29ac5087
Source dataset
uspto-grants-1996_10
Patent number
US05567717

Linked notes

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