Ethyl Bromide → 6-(3-ethoxyphenyl)-2-ethyl-3(2H)-pyridazinone

HRID 1954001ノート

反応式

HRID 1954001 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([C:8]2[CH:9]=[CH:10][C:11](=[O:14])[NH:12][N:13]=2)[CH:5]=[CH:6][CH:7]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:21](Br)[CH3:22].N1N[C:26](=O)[CH:27]=CC=1>C(O)C>[CH2:26]([O:1][C:2]1[CH:3]=[C:4]([C:8]2[CH:9]=[CH:10][C:11](=[O:14])[N:12]([CH2:21][CH3:22])[N:13]=2)[CH:5]=[CH:6][CH:7]=1)[CH3:27]

参加物

6

実験手順

To a 2 liter 4-neck round bottom flask, stirring under a nitrogen atomsphere, was charged 50.0 g (1.0 eq., 0.266 moles) of 6-(3-hydroxyphenyl)-3(2H)-pyridazinone in 500 ml of ethanol followed by 73.4 g of potassium carbonate (2.0 eq., 0.53 moles) and 58.0 g of ethyl bromide (2.0 eq., 0.53 moles) in 50 ml of ethanol. The reaction was stirred at reflux, 70° C.-72° C. for 6 hr. with monitoring by glc. After 6 hr. 5.8 g of ethylbromide was added (0.2 eq., 53 mmoles) and after stirring for an addtional 15 hr. at reflux glc indicated all the starting pyridazinone was consumed. The reaction was worked up by vacuum filtering the mixture while still warm and washing the solid with 2×150 ml of ethanol. The filtrate was concentrated by evaporation under reduced pressure to afford 67.3 g of 6-(3-ethoxyphenyl)-2-ethyl-3(2H)-pyridazinone as a brown oil which solidified.

後処理

  1. stirringThe reaction was stirred
  2. temperatureat reflux, 70° C.-72° C. for 6 hr
  3. stirringafter stirring for an addtional 15 hr
  4. temperatureat reflux glc
  5. customwas consumed
  6. filtrationfiltering the mixture
  7. temperaturewhile still warm
  8. washwashing the solid with 2×150 ml of ethanol
  9. concentrationThe filtrate was concentrated by evaporation under reduced pressure

出典と根拠

ORDレコード
ord-9d11393bb9814784b6d9541792bf362a
出典データセット
uspto-grants-2000_09
特許番号
US06121251

反応ノート

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