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3-Bromopyridine → 3-Cyclopentylpyridine

HRID 2212078
ノート
印刷プレビュー

反応式

HRID 2212078 の反応式
Br[C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1.[CH:8]1([Mg]Cl)[CH2:12][CH2:11][CH2:10][CH2:9]1>O1CCCC1.C1C=CC(P(C2C=CC=CC=2)CCP(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.Cl[Ni]Cl>[CH:8]1([C:2]2[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=2)[CH2:12][CH2:11][CH2:10][CH2:9]1
参加物反応条件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 122863-BromopyridineHCID 178478989HCID 178478989、化合物2 回

生成物 1

HCID 219638603-Cyclopentylpyridine収率 30%

試薬・触媒・溶媒 2

HCID 2734542[1,2-Bis(diphenylphosphino)ethane]dichloronickel(II)触媒HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-5 °C

実験手順

3-Bromopyridine (3.9 ml, 40 mmol) and [1,2-bis(diphenylphosphino)ethane]dichloronickel(II) (160 mg, 0.3 mmol) were dissolved in dry tetrahydrofuran (25 ml) and cooled to −5° C. Cyclopentylmagnesium chloride (2.0M in diethyl ether, 20 ml, 40 mmol) was added dropwise over 5–10 minutes and the reaction was allowed to warm slowly to room temperature. Further cyclopentylmagnesium chloride (2.0M in diethyl ether, 5 ml, 10 mmol) was added. The reaction was quenched by the addition of saturated aqueous ammonium chloride solution. The mixture was partitioned between water and ethyl acetate. The organic layer was dried (MgSO4) and concentrated in vacuo. The residue was purified by flash column chromatography on silica, eluting with 20–35% ethyl acetate/i-hexane, to give the title compound (1.74 g, 30%).

後処理

  1. temperatureto warm slowly to room temperature
  2. customThe reaction was quenched by the addition of saturated aqueous ammonium chloride solution
  3. customThe mixture was partitioned between water and ethyl acetate
  4. dry with materialThe organic layer was dried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by flash column chromatography on silica
  7. washeluting with 20–35% ethyl acetate/i-hexane

出典と根拠

ORDレコード
ord-27dc71682f4e4c5c9ea1b348d408e5df
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07101892B2

反応ノート

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