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Methyl bromoacetate → HCID 18369422、化合物

HRID 1699770
ノート
印刷プレビュー

反応式

HRID 1699770 の反応式
[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][C:8]([C:10]2[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=2)=[O:9])=[CH:3][CH:2]=1.C([N-]C(C)C)(C)C.[Li+].Br[CH2:27][C:28]([O:30][CH3:31])=[O:29]>O1CCCC1.C1(C)C=CC=CC=1>[CH3:17][O:16][C:13]1[CH:12]=[CH:11][C:10]([C:8](=[O:9])[CH:7]([C:4]2[CH:5]=[CH:6][N:1]=[CH:2][CH:3]=2)[CH2:27][C:28]([O:30][CH3:31])=[O:29])=[CH:15][CH:14]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 60984Methyl bromoacetateHCID 2724682Lithium diisopropylamideHCID 100824531-(4-Methoxyphenyl)-2-(pyridin-4-yl)ethanone

生成物 1

HCID 18369422HCID 18369422、化合物

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

Under an argon, 2-(4-pyridyl)-4′-methoxyacetophenone (J. Am. Chem. Soc., 112, 2163-3168, 1990: Dimitrios Stefanidis and John W. Bunting; 9.6 g, 42.3 mmol) was suspended in tetrahydrofuran (200 ml), and under ice cooling, lithium diisopropylamide (2.0 M solution; 25 ml, 50.0 mmol) was added. At the same temperature, the mixture was stirred for 30 minutes. Methyl bromoacetate (6.0 ml, 63.4 mmol) was then added dropwise, and the mixture was stirred under ice cooling for 1 hour and then at room temperature for 2 hours. The reaction mixture was diluted with toluene. The mixture was washed successively with 2 N hydrochloric acid, water and a brine, and was then dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was separated and purified by chromatography on a silica gel column [silica gel: 100 g, hexane/ethyl acetate (1/2)], whereby the title compound (10.63 g, 84.1%) was obtained as a brown oil.

後処理

  1. stirringthe mixture was stirred under ice cooling for 1 hour
  2. waitat room temperature for 2 hours
  3. washThe mixture was washed successively with 2 N hydrochloric acid, water
  4. dry with materiala brine, and was then dried over anhydrous sodium sulfate
  5. distillationThe solvent was distilled off
  6. customthe residue was separated
  7. custompurified by chromatography on a silica gel column [silica gel: 100 g, hexane/ethyl acetate (1/2)], whereby the title compound (10.63 g, 84.1%)
  8. customwas obtained as a brown oil

出典と根拠

ORDレコード
ord-98138e12ebea4a45b98a5c8e4f2ad6a1
出典データセット
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06348468B1

反応ノート

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