Diethyl Malonate → Diethyl 2-(5-nitropyridin-2-yl)malonate

HRID 374418ノート

反応式

HRID 374418 の反応式
[C:1]([O:9][CH2:10][CH3:11])(=[O:8])[CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4].[H-].[Na+].Cl[C:15]1[CH:20]=[CH:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][N:16]=1>O1CCCC1>[N+:21]([C:18]1[CH:19]=[CH:20][C:15]([CH:2]([C:3]([O:5][CH2:6][CH3:7])=[O:4])[C:1]([O:9][CH2:10][CH3:11])=[O:8])=[N:16][CH:17]=1)([O-:23])=[O:22]

参加物

5

反応条件

温度
60 °C

実験手順

Diethyl malonate (74 g) was added to a stirred suspension of sodium hydride (60% dispersion in oil; 18 g) in dry tetrahydrofuran under an inert atmosphere. The resulting suspension was stirred at reflux for one hour. The mixture was cooled to 60° C. and a solution of 2-chloro-5-nitropyridine (50 g) in dry tetrahydrofuran was added. The resulting red solution was stirred at reflux for 3 hours then allowed to stand at room temperature overnight. The volume of solvent was reduced by evaporation, water was added to the residue and the mixture was acidified to pH 1 with concentrated hydrochloric acid. The mixture was extracted with ethyl acetate, washed with water, dried (anhydrous magnesium sulphate), filtered and evaporated. The crude product was triturated in a mixture of cyclohexane and diethyl ether to yield diethyl 2-(5-nitropyridin-2-yl)malonate (56.5 g) as a yellow solid, m.p. 91.5°-93.5° C.

後処理

  1. temperatureat reflux for one hour
  2. stirringThe resulting red solution was stirred
  3. temperatureat reflux for 3 hours
  4. customThe volume of solvent was reduced by evaporation, water
  5. additionwas added to the residue
  6. extractionThe mixture was extracted with ethyl acetate
  7. washwashed with water
  8. dry with materialdried (anhydrous magnesium sulphate)
  9. filtrationfiltered
  10. customevaporated
  11. customThe crude product was triturated in a mixture of cyclohexane and diethyl ether

出典と根拠

ORDレコード
ord-083cab1b1ace4f1199defcbca01b8670
出典データセット
uspto-grants-1996_01
特許番号
US05480857

反応ノート

読み込み中…