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Borane → HCID 11096444、化合物

HRID 1741813
ノート
印刷プレビュー

反応式

HRID 1741813 の反応式
[CH:1]1[CH:2]=[C:3]([C:10](=O)[CH2:11][CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14])[N:4]2[C:9]=1[CH:8]=[CH:7][CH:6]=[CH:5]2.B>O1CCCC1>[CH:1]1[CH:2]=[C:3]([CH2:10][CH2:11][CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14])[N:4]2[C:9]=1[CH:8]=[CH:7][CH:6]=[CH:5]2
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6331BoraneHCID 10879379Ethyl 4-(3-indolizinyl)-4-oxobutyrate

生成物 1

HCID 11096444HCID 11096444、化合物収率 56.1%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a solution of ethyl 4-(3-indolizinyl)-4-oxobutyrate (556 mg) in tetrahydrofuran (5 ml) was added borane in tetrahydrofuran (1M solution, 3.6 ml) at 0° C. After stirring at room temperature for 10 minutes, the reaction was quenched by aqueous potassium dihydrogen phosphate at 0° C., and the resulting mixture was extracted with ether. The organic layers were washed with water, aqueous sodium bicarbonate and brine, dried over sodium sulfate. After evaporation of the solvent, the residue was chromatographed on alumina (Hexane-methylene chloride=1:1) to give ethyl 4-(3-indolizinyl)butyrate (294 mg).

後処理

  1. customthe reaction was quenched by aqueous potassium dihydrogen phosphate at 0° C.
  2. extractionthe resulting mixture was extracted with ether
  3. washThe organic layers were washed with water, aqueous sodium bicarbonate and brine
  4. dry with materialdried over sodium sulfate
  5. customAfter evaporation of the solvent
  6. customthe residue was chromatographed on alumina (Hexane-methylene chloride=1:1)

出典と根拠

ORDレコード
ord-f8076d5d04c8405ab1a80e5204d39e80
出典データセット
uspto-grants-1994_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05334716

反応ノート

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