Potassium Cyanide → 2-Cyano-5,6-dimethoxy-indan-1-one

HRID 247015ノート

反応式

HRID 247015 の反応式
Br[CH:2]1[CH2:10][C:9]2[C:4](=[CH:5][C:6]([O:13][CH3:14])=[C:7]([O:11][CH3:12])[CH:8]=2)[C:3]1=[O:15].[C-:16]#[N:17].[K+]>C(O)C.O>[C:16]([CH:2]1[CH2:10][C:9]2[C:4](=[CH:5][C:6]([O:13][CH3:14])=[C:7]([O:11][CH3:12])[CH:8]=2)[C:3]1=[O:15])#[N:17]

参加物

5

実験手順

2-Bromo-5,6-dimethoxy-indan-1-one (69.1 g) was suspended in ethanol (1,200 ml) and added to a solution of potassium cyanide (70.4 g) in water (2,200 ml). The reaction mixture was heated at reflux for 1 hour and then the ethanol was distilled off. The dark solution was cooled, stirred and carefully neutralised with hydrochloric acid (5M, 120 ml) in a well ventilated hood. The organic extracts were combined, washed with brine, dried over magnesium sulphate, filtered, then concentrated to low volume under reduced pressure. The residual liquid was filtered through a column of coarse silica (0.2-0.5 mm, Merck, 300 g) and the column was eluted with dichloromethane. The appropriate fractions were combined and evaporated to dryness to give 2-Cyano-5,6-dimethoxy-indan-1-one (24.6 g). A portion crystallised from dichloromethane: ether; m.p. 177°-179° C.

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 1 hour
  3. distillationthe ethanol was distilled off
  4. temperatureThe dark solution was cooled
  5. washwashed with brine
  6. dry with materialdried over magnesium sulphate
  7. filtrationfiltered
  8. concentrationconcentrated to low volume under reduced pressure
  9. filtrationThe residual liquid was filtered through a column of coarse silica (0.2-0.5 mm, Merck, 300 g)
  10. washthe column was eluted with dichloromethane
  11. customevaporated to dryness

出典と根拠

ORDレコード
ord-11ece82495d24af4b251a3f6e7188615
出典データセット
uspto-grants-1987_11
特許番号
US04705782

反応ノート

読み込み中…