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Gamma-Butyrolactone → 4-Hydroxy-1-(3-pyridyl)-1-butanone

HRID 1030598
ノート
印刷プレビュー

反応式

HRID 1030598 の反応式
Br[C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1.CCCCCC.C([Li])CCC.[C:19]1(=[O:24])[O:23][CH2:22][CH2:21][CH2:20]1>CCOCC>[N:4]1[CH:5]=[CH:6][CH:7]=[C:2]([C:22](=[O:23])[CH2:21][CH2:20][CH2:19][OH:24])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 7302Gamma-ButyrolactoneHCID 122863-BromopyridineHCID 178418244HCID 178418244、化合物

生成物 1

HCID 1078194-Hydroxy-1-(3-pyridyl)-1-butanone収率 77%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

実験手順

A solution of 10.0 g (63.3 mmol) of 3-bromopyridine in 100 ml of ether was cooled to -78° C., to which 40 ml (64 mmol) of 1.6 M n-butyllithium hexane solution was added dropwise with stirring. After completion cf the addition, the mixture was stirred for further 15 minutes, to which the solution of 5.45 g (63.3 mmol) of γ-butyrolactone in 15 ml of ether was added dropwise, and stirred for further 1 hour at -78° C.-room temperature. To the reaction mixture an aqueous solution of ammonium chloride, and the resultant substance was extracted with ethyl acetate. The extract was washed with water and dried, and the solvent was evaporated off. The residue was purified with silica gel column chromatography (CHCl3 -MeOH (9:1)) and recrystallized from ethyl acetate-isopropyl ether, to give 8.0 g (77%) of 4-(3-pyridyl)-4-oxobutanol. m.p. 36°-37° C.

後処理

  1. additionwas added dropwise
  2. additionAfter completion cf the addition
  3. additionwas added dropwise
  4. stirringstirred for further 1 hour at -78° C.-room temperature
  5. extractionTo the reaction mixture an aqueous solution of ammonium chloride, and the resultant substance was extracted with ethyl acetate
  6. washThe extract was washed with water
  7. customdried
  8. customthe solvent was evaporated off
  9. customThe residue was purified with silica gel column chromatography (CHCl3 -MeOH (9:1))
  10. customrecrystallized from ethyl acetate-isopropyl ether

出典と根拠

ORDレコード
ord-7d195b6cc6ba41b6973ce1b532a4257e
出典データセット
uspto-grants-1992_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05106858

反応ノート

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