Carbon Dioxide → Sodium tetrahydropyran-2-yloxyethanoate

HRID 5912ノート

反応式

HRID 5912 の反応式
O1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][CH2:8]C#N.[OH-:11].[Na+:12].[C:13](=[O:15])=[O:14]>C(O)C.C(#N)C>[O:11]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][CH2:8][C:13]([O-:15])=[O:14].[Na+:12]

参加物

6

実験手順

To a solution of tetrahydropyran-2-yloxyethanonitrile (6.0 g, 42.49 mmol) in ethanol (15 ml) was added aqueous sodium hydroxide solution (10M, 15 ml). Following the initial exothermic reaction the solution was heated under reflux for 1.5 hours, diluted with ethanol (30 ml) and the pH adjusted to 8 by the addition of carbon dioxide pellets. The resulting gelatinous suspension was diluted with acetonitrile (60 ml), filtered at 60° C. through diatomaceous earth and the insoluble material extracted in a similar manner with a mixture of acetonitrile/ethanol/water (4:3:1, 2×120 ml). The crude product was purified by dissolution in warm isopropanol, filtration at 0° C. through diatomaceous earth, evaporation of the solvent in vacuo and trituration of the residue with acetone at 0° C. to yield sodium tetrahydropyran-2-yloxyethanoate (6.24 g, 34.26 mmol) as a colorless powder, m.p. 198°-205° C.;

後処理

  1. customexothermic reaction the solution
  2. temperaturewas heated
  3. temperatureunder reflux for 1.5 hours
  4. filtrationfiltered at 60° C. through diatomaceous earth
  5. extractionthe insoluble material extracted in a similar manner with a mixture of acetonitrile/ethanol/water (4:3:1, 2×120 ml)
  6. customThe crude product was purified by dissolution in warm isopropanol
  7. filtrationfiltration at 0° C.
  8. customthrough diatomaceous earth, evaporation of the solvent in vacuo and trituration of the residue with acetone at 0° C.

出典と根拠

ORDレコード
ord-56f6f1a3df2341c1b4970df530132daa
出典データセット
uspto-grants-1993_09
特許番号
US05246950

反応ノート

読み込み中…