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Potassium Fluoride → HCID 15811458、化合物

HRID 868769
ノート
印刷プレビュー

反応式

HRID 868769 の反応式
C[Si]([C:5]#[C:6][C:7]1[CH:8]=[CH:9][C:10]([C:13]2[CH:18]=[CH:17][C:16]([C:19]#[C:20][Si](C)(C)C)=[CH:15][N:14]=2)=[N:11][CH:12]=1)(C)C.[F-].[K+]>CO.C1COCC1>[C:19]([C:16]1[CH:17]=[CH:18][C:13]([C:10]2[CH:9]=[CH:8][C:7]([C:6]#[CH:5])=[CH:12][N:11]=2)=[N:14][CH:15]=1)#[CH:20]
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 2

HCID 522689Potassium FluorideHCID 52476625,5'-Bis(trimethylsilylethynyl)-2,2'-bipyridine

生成物 1

HCID 15811458HCID 15811458、化合物

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

4 (390 mg, 1.12 mmol) was dissolved in a mixture of 40 ml MeOH and 10 ml THF; then KF powder (400 mg, 6.88 mmol) was added and the solution was stirred at room temperature overnight. Subsequently, the solvents were removed under reduced pressure. The residue was redissolved in 200 ml CH2Cl2 and washed four times with 100 ml H2O each, in order to remove inorganic salts. The organic phase was dried over Na2SO4, concentrated under reduced pressure and purified by silica flash column chromatography (eluent: CH2Cl2) to yield a colorless powder of 204 mg (1.0 mmol, 81%) pure 5. 1H NMR (CDCl3, 250 MHz): δ=8.76 (d, 2H, JHH=1.0 Hz, bpy-H), 8.39 (d, 2H, JHH=6.0 Hz, bpy-H), 7.90 (dd, 2H, JHH=1.1 Hz, 5.1 Hz, bpy-H), 3.31 (s, 2H, bpy-CCH).

後処理

  1. customSubsequently, the solvents were removed under reduced pressure
  2. dissolutionThe residue was redissolved in 200 ml CH2Cl2
  3. washwashed four times with 100 ml H2O each, in order
  4. customto remove inorganic salts
  5. dry with materialThe organic phase was dried over Na2SO4
  6. concentrationconcentrated under reduced pressure
  7. custompurified by silica flash column chromatography (eluent: CH2Cl2)
  8. customto yield a colorless powder of 204 mg (1.0 mmol, 81%) pure 5

出典と根拠

ORDレコード
ord-1513561857dc4ebeb902cb5959c561aa
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08968886B2

反応ノート

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