Ethyl Bromide → 6-(3-ethoxyphenyl)-2-ethyl-3(2H)-pyridazinone
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
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
- stirringThe reaction was stirred
- temperatureat reflux, 70° C.-72° C. for 6 hr
- stirringafter stirring for an addtional 15 hr
- temperatureat reflux glc
- customwas consumed
- filtrationfiltering the mixture
- temperaturewhile still warm
- washwashing the solid with 2×150 ml of ethanol
- 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
読み込み中…