Ammonia → 2-Amino-2-methyl-indan-1-one

HRID 244785

反応式

HRID 244785 の反応式
[CH3:1][CH:2]1[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]1=[O:11].[NH3:12].[OH-].[Na+]>O>[NH2:12][C:2]1([CH3:1])[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]1=[O:11]

参加物

5

反応条件

温度
80 °C

実験手順

According to the procedure of Farnum et. al (Synthesis 1972, 191-192.), water (1.35 L) is stirred at 80° C. and de-gassed by periodic evacuating and flushing with nitrogen (3×). K3FeCN6 (202 g, 615 mmol) and 2-methyl-indan-1-one (20 g, 137 mmol) are added. The mixture is stirred rapidly under nitrogen at 80° C. while aqueous concentrated ammonia solution (105 mL) is added over 30 minutes. Stirring is continued at 80° C. for 20 hours. When cool, the solution is made alkaline by addition of sodium hydroxide (2 g) and extracted with ethyl acetate (2×200 mL). The organic extract is concentrated to a volume of 200 ml and the product is extracted into aqueous HCl (200 mL, 1M). The acidic aqueous phase is separated, basified with sodium hydroxide, and extracted with ethyl acetate (2×100 mL). The organic layer is separated, dried (Na2SO4) and the solvent removed to give an orange oil.

後処理

  1. customde-gassed
  2. customby periodic evacuating
  3. customflushing with nitrogen (3×)
  4. additionis added over 30 minutes
  5. stirringStirring
  6. temperatureWhen cool
  7. extractionextracted with ethyl acetate (2×200 mL)
  8. extractionThe organic extract
  9. concentrationis concentrated to a volume of 200 ml
  10. extractionthe product is extracted into aqueous HCl (200 mL, 1M)
  11. customThe acidic aqueous phase is separated
  12. extractionextracted with ethyl acetate (2×100 mL)
  13. customThe organic layer is separated
  14. dry with materialdried (Na2SO4)
  15. customthe solvent removed
  16. customto give an orange oil

出典と根拠

ORDレコード
ord-63f350d37d6440c8823a7d1fe8a93a26
出典データセット
uspto-grants-2014_02
特許番号
US08658673B2

関連ノート

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