Sodium Hydroxide → 1-Methyl-1,10-phenanthrolin-2(1H)-one

HRID 241392

反応式

HRID 241392 の反応式
[I-].[CH3:2][N+:3]1[C:16]2[C:7](=[CH:8][CH:9]=[C:10]3[C:15]=2[N:14]=[CH:13][CH:12]=[CH:11]3)[CH:6]=[CH:5][CH:4]=1.[OH-:17].[Na+]>[Fe-3](C#N)(C#N)(C#N)(C#N)(C#N)C#N.[K+].[K+].[K+]>[CH3:2][N:3]1[C:16]2[C:7](=[CH:8][CH:9]=[C:10]3[C:15]=2[N:14]=[CH:13][CH:12]=[CH:11]3)[CH:6]=[CH:5][C:4]1=[O:17]

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 117716101-Methyl-1,10-phenanthrolinium iodide

生成物 1

HCID 35813871-Methyl-1,10-phenanthrolin-2(1H)-one収率 96.4%

試薬・触媒・溶媒 1

HCID 178511488HCID 178511488、化合物触媒

実験手順

To a stirred aqueous solution of potassium ferricyanide (92.2 g; 280 mmol) (1.12L), compound (1) (37.6 g; 117 mmol) and an aqueous solution of sodium hydroxide (69.3 g; 1.73 mol) (200 mL) were alternately added in an ice bath (inner temperature of 10 to 15° C.) over 20 minutes. The resulting reaction mixture was stirred at room temperature for 3 hours. Crude crystals which precipitated out were filtered out and dried. The resulting crude crystals were dissolved in toluene (1.1 L) and benzene (450 mL), and insoluble matters were filtrated out. The filtrate was evaporated under reduced pressure, and the resulting residue was washed with isopropyl ether and ethyl acetate, and then dried to give 23.7 g (yield: 75%) of the title compound (2).

後処理

  1. customThe resulting reaction mixture
  2. customCrude crystals which precipitated out
  3. filtrationwere filtered out
  4. customdried
  5. dissolutionThe resulting crude crystals were dissolved in toluene (1.1 L)
  6. filtrationbenzene (450 mL), and insoluble matters were filtrated out
  7. customThe filtrate was evaporated under reduced pressure
  8. washthe resulting residue was washed with isopropyl ether and ethyl acetate
  9. customdried

出典と根拠

ORDレコード
ord-77860796842f444ebb053961dbde0dab
出典データセット
uspto-grants-2014_02
特許番号
US08648194B2

関連ノート

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