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Boron trifluoride etherate → HCID 56763784、化合物

HRID 1672068
ノート
印刷プレビュー

反応式

HRID 1672068 の反応式
[O:1]1[CH:5]=[CH:4][C:3]([C:6]#[N:7])=[CH:2]1.[CH2:8]([Mg]Br)[CH3:9].B(F)(F)F.CCOCC.[OH-].[Na+]>C1COCC1.CC(C)[O-].[Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-]>[O:1]1[CH:5]=[CH:4][C:3]([C:6]2([NH2:7])[CH2:9][CH2:8]2)=[CH:2]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 8000Boron trifluoride etherateHCID 14798Sodium HydroxideHCID 1006983-Furancarbonitrile (9CI)HCID 178418443HCID 178418443、化合物

生成物 1

HCID 56763784HCID 56763784、化合物

試薬・触媒・溶媒 2

HCID 11026Titanium isopropoxide触媒
HCID 8028
Tetrahydrofuran
溶媒
2 回

実験手順

To solution of 3-furonitrile (5 g, 53.71 mmol, 1.0 eq) in dry THF at r.t. under an argon atmosphere was added slowly titanium isopropoxide (18.9 ml, 64.4 mmol, 1.2 eq). The reaction mixture was stirred for 15 min. A solution of 1.0 M ethyl magnesium bromide in THF (129 ml, 128 mmol, 2.4 eq) was added via syringe slowly to the mixture at 0° C. After addition, the reaction mixture was stirred at r.t. for 2 hour. BF3.Et2O (10.4 ml) was then added slowly to the mixture at 0° C. After completion of the addition, the reaction mixture was stirred at r.t. for 30 min. 10% NaOH solution was added slowly till the reaction mixture becomes basic and then extracted with EtOAC. The organic was washed with brine, dried over Na2SO4 and concentrated. The crude product was purified by silica gel (60-120) column chromatography using 35% EtOAC/pet ether as eluent. Yield: 2.5 g (38%). 1F NMR (400 MHz, CDCl3): δ 7.32 (m, 2H), 6.10 (s, 1H), 0.98-0.95 (m, 2H), 0.83-0.78 (m, 2H). LCMS: (ES+) m/z=123.7 (M)+

後処理

  1. additionAfter addition
  2. stirringthe reaction mixture was stirred at r.t. for 2 hour
  3. additionAfter completion of the addition
  4. stirringthe reaction mixture was stirred at r.t. for 30 min
  5. extractionextracted with EtOAC
  6. washThe organic was washed with brine
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated
  9. customThe crude product was purified by silica gel (60-120) column chromatography

出典と根拠

ORDレコード
ord-5a2a2ebf95454e4e8dcea068697d68c6
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07994171B2

反応ノート

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