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

HRID 439330

反応式

HRID 439330 の反応式
[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>[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

参加物

6

実験手順

A mixture of 4 mL (139.6 mmol) 2-acetylfuran, 8.7 mL (156 mmol) of ethylene glycol, 198 mg (1 mmol) of ptoluenesulfonic 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 tort) 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 min.

後処理

  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 tort)

出典と根拠

ORDレコード
ord-84b3147593fa4b128550e1ee6d74426a
出典データセット
uspto-grants-1996_05
特許番号
US05514679

関連ノート

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