Sodium Bicarbonate → 1-amino-2,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-indene

HRID 330245

反応式

HRID 330245 の反応式
[CH3:1][C:2]1[CH:10]=[C:9]([CH3:11])[C:8]([OH:12])=[C:7]2[C:3]=1[CH2:4][CH:5]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:6]2=[N:13]O.[H][H].C(=O)(O)[O-].[Na+]>C(O)(=O)C.O.[Pt]=O>[NH2:13][CH:6]1[C:7]2[C:3](=[C:2]([CH3:1])[CH:10]=[C:9]([CH3:11])[C:8]=2[OH:12])[CH2:4][CH:5]1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

参加物

7

反応物 3

HCID 516892Sodium BicarbonateHCID 1363428322,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-inden-1-one oximeHCID 178418361HCID 178418361、化合物

生成物 1

HCID 140303341-amino-2,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-indene

試薬・触媒・溶媒 3

HCID 82844Platinum oxide (PtO)触媒HCID 176Acetic Acid溶媒HCID 962Water溶媒

実験手順

3.00 Grams of 2,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-inden-1-one oxime was dissolved in 55 ml of glacial acetic acid, and this solution was subjected to catalytic hydrogenation in the presence of 0.3 g of platinum oxide at room temperature under 4 atmospheric hydrogen gas pressure. The hydrogenation was terminated at the point when the stoichiometric amount of hydrogen was absorbed. The catalyst was removed by filtration and the filtrate thus obtained was concentrated. The residue thus obtained was dissolved in water and the pH of this solution was adjusted to about pH 8 by adding an aqueous solution of sodium bicarbonate, then extracted with 200 ml of chloroform. The chloroform extract was washed with water, dried with anhydrous magnesium sulfate, then concentrated under a reduced pressure. Recrystallized from ethanol to obtain 0.24 g of 1-amino-2,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-indene. Colorless needle-like crystals. Melting point: 135°-136° C.

後処理

  1. customThe hydrogenation was terminated at the point when the stoichiometric amount of hydrogen
  2. customwas absorbed
  3. customThe catalyst was removed by filtration
  4. customthe filtrate thus obtained
  5. concentrationwas concentrated
  6. customThe residue thus obtained
  7. extractionextracted with 200 ml of chloroform
  8. extractionThe chloroform extract
  9. washwas washed with water
  10. dry with materialdried with anhydrous magnesium sulfate
  11. concentrationconcentrated under a reduced pressure
  12. customRecrystallized from ethanol

出典と根拠

ORDレコード
ord-ccdc767980c948329a7da75b51dc494d
出典データセット
uspto-grants-1990_01
特許番号
US04895847

関連ノート

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