Acetic Acid → Indoxyl acetate

HRID 641885

反応式

HRID 641885 の反応式
I[C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[NH:4][CH:3]=1.[C:11]([OH:14])(=[O:13])[CH3:12]>>[C:11]([O:14][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[NH:4][CH:3]=1)(=[O:13])[CH3:12]

参加物

3

反応条件

温度
90 °C

実験手順

Into a 500 mL round bottom flask was placed a solution of 3-iodo-1H-indole (23 g, 94.65 mmol) in acetic acid (300 mL). To the mixture was added CH3COOAg (31.6 g, 189.22 mmol). The resulting solution was allowed to react, with stirring, for 1 hour while the temperature was maintained at 90° C. in a bath of oil. The reaction progress was monitored by TLC (ethyl acetate/petroleum ether=1:1). A filtration was performed. The filtrate was concentrated by evaporation under vacuum using a rotary evaporator. The resulting solution was dissolved with 100 mL of ethyl acetate. The resulting mixture was washed 2 times with 100 mL of NaCl(aq.). The final product was purified by recrystallization from MeOH/H2O in the ratio 2:3. This resulted in 8.5 g (41%) of 1H-indol-3-yl acetate as a dark purple solid.

後処理

  1. customInto a 500 mL round bottom flask was placed
  2. additionTo the mixture was added CH3COOAg (31.6 g, 189.22 mmol)
  3. customto react
  4. filtrationA filtration
  5. concentrationThe filtrate was concentrated by evaporation under vacuum
  6. customa rotary evaporator
  7. dissolutionThe resulting solution was dissolved with 100 mL of ethyl acetate
  8. washThe resulting mixture was washed 2 times with 100 mL of NaCl(aq.)
  9. customThe final product was purified by recrystallization from MeOH/H2O in the ratio 2:3
  10. customThis resulted in 8.5 g (41%) of 1H-indol-3-yl acetate as a dark purple solid

出典と根拠

ORDレコード
ord-e5cb03474d334acf95b8db8792e2cd23
出典データセット
uspto-grants-2010_04
特許番号
US07696229B2

関連ノート

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