Ethanol → 3-(Acetyloxy)butanoic acid

HRID 727966ノート

反応式

HRID 727966 の反応式
O.[OH-].[Na+].[OH:4][C@H:5]([CH3:12])[CH2:6][C:7]([O:9]CC)=[O:8].[Cl-].[Na+].[CH2:15]([OH:17])[CH3:16]>>[C:15]([O:4][CH:5]([CH3:12])[CH2:6][C:7]([OH:9])=[O:8])(=[O:17])[CH3:16]

参加物

6

実験手順

In a liquid mixture comprising 15 ml of water, 15 ml of ethanol and sodium hydroxide was dissolved 4.0 of ethyl (R)-β-hydroxybutanoate, and the solution was refluxed under heating, cooled and passed through an ion exchange resin (Amberlite1/2 IR-120B). The solvent was removed under a reduced pressure, 10 ml of anhydrous pyridine and 3 ml of anhydrous acetic acid were added to the residue, and the mixture was stirred at room temperature overnight. Dilute hydrochloric acid was added to the reaction liquid to adjust the pH value to 1, and the reaction liquid was saturated with sodium chloride and extracted with chloroform. The extract was washed with a saturated aqueous sodium chloride solution and dehydrated on magnesium sulfate. Then, chloroform was removed under a reduced pressure to obtain 3.6 g of the intended compound having [α]24 of -5.7°.

後処理

  1. temperaturethe solution was refluxed
  2. temperatureunder heating
  3. temperaturecooled
  4. customThe solvent was removed under a reduced pressure, 10 ml of anhydrous pyridine and 3 ml of anhydrous acetic acid
  5. additionwere added to the residue
  6. additionDilute hydrochloric acid was added to the reaction liquid
  7. customthe reaction liquid
  8. extractionextracted with chloroform
  9. washThe extract was washed with a saturated aqueous sodium chloride solution
  10. customThen, chloroform was removed under a reduced pressure

出典と根拠

ORDレコード
ord-fa082a670e2d471382eb660b2509ab74
出典データセット
uspto-grants-1991_09
特許番号
US05045228

反応ノート

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