3-Methyl-2-butanone → 2,3,3-Trimethyl-3H-indole-5-carboxylic acid

HRID 61514

反応式

HRID 61514 の反応式
[NH:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][CH:4]=1)N.[CH:12]([C:15]([CH3:17])=O)([CH3:14])[CH3:13]>C(O)(=O)C>[CH3:17][C:15]1[C:12]([CH3:14])([CH3:13])[C:11]2[C:3](=[CH:4][CH:5]=[C:6]([C:7]([OH:9])=[O:8])[CH:10]=2)[N:1]=1

参加物

4

反応物 2

HCID 112513-Methyl-2-butanoneHCID 120894-Hydrazinobenzoic acid

生成物 1

HCID 30196962,3,3-Trimethyl-3H-indole-5-carboxylic acid収率 80.1%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

A solution of 4-hydrazinobenzoic acid (10.0 g, 65.7 mmol), isopropylmethylketone (21.1 mL, 197 mmol) in acetic acid (35 mL) was heated under reflux in an oil bath for 20 h. After cooling to ambient temperature the solvent was evaporated off under reduced pressure and to it was added a saturated aqueous solution of NaHCO3 (50 mL) and washed with CH2Cl2 (3×40 mL). The pH of the aqueous solution was adjusted with 1 M aqueous HCl to ca. 2, and then extracted with CH2Cl2 (3×50 mL). The combined organic solution was then dried with Na2SO4, filtered and concentrated to dryness under reduced pressure to yield the desired product (10.7 g, 80%) as a brownish solid. (This is also [0147] 1.1)

後処理

  1. temperatureunder reflux in an oil bath for 20 h
  2. customwas evaporated off under reduced pressure and to it
  3. additionwas added a saturated aqueous solution of NaHCO3 (50 mL)
  4. washwashed with CH2Cl2 (3×40 mL)
  5. extractionextracted with CH2Cl2 (3×50 mL)
  6. dry with materialThe combined organic solution was then dried with Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated to dryness under reduced pressure

出典と根拠

ORDレコード
ord-815f62d2fcad4523acd850d4becc56d6
出典データセット
uspto-grants-2016_09
特許番号
US09441270B2

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