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Dichloromethane → 6-Ethenylpyridine-3-carbonitrile

HRID 515114
ノート
印刷プレビュー

反応式

HRID 515114 の反応式
Br[C:2]1[N:7]=[CH:6][C:5]([C:8]#[N:9])=[CH:4][CH:3]=1.ClCCl.[CH2:13](N(CC)CC)[CH3:14].C(OCC)(=O)C>CCO.O>[CH:13]([C:2]1[N:7]=[CH:6][C:5]([C:8]#[N:9])=[CH:4][CH:3]=1)=[CH2:14]
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 6344DichloromethaneHCID 8471TriethylamineHCID 8857Ethyl AcetateHCID 50057186-Bromopyridine-3-carbonitrile

生成物 1

HCID 190453106-Ethenylpyridine-3-carbonitrile

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962
Water
溶媒
2 回

実験手順

To a stirring solution of 6-bromopyridine-3-carbonitrile (2.0 g, 10.9 mmol), in EtOH (70 mL) were added bis[(diphenylphosphino)ferrocene]dichloropalladium(II) complex with dichloromethane (0.892 mg, 0.10 mmol), potassium vinyl trifluoroborate (2.93 g, 21.9 mmol), triethylamine (3.0 mL, 21.9 mmol), and water (0.5 mL). The reaction mixture was heated to reflux. Upon completion as determined by reverse phase HPLC-MS (1-2 h) and TLC (eluent: 10% ethyl acetate in hexanes), the reaction was cooled to room temperature, and then was diluted with water and extracted with EtOAc. The combined organic layers were washed with brine and dried over MgSO4. The extracts were concentrated and chromatographed over a column of SiO2 (0-20% EtOAc hexanes as eluent). Evaporation of the solvent yielded 6-ethenylpyridine-3-carbonitrile.

後処理

  1. temperatureThe reaction mixture was heated to reflux
  2. extractionextracted with EtOAc
  3. washThe combined organic layers were washed with brine
  4. dry with materialdried over MgSO4
  5. concentrationThe extracts were concentrated
  6. customchromatographed over a column of SiO2 (0-20% EtOAc hexanes as eluent)
  7. customEvaporation of the solvent

出典と根拠

ORDレコード
ord-3f630486f392455a97d517bd40fc8bd5
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09108947B2

反応ノート

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