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Pyridine → 3-Acetyl-4-fluorobenzonitrile

HRID 398358
ノート
印刷プレビュー

反応式

HRID 398358 の反応式
N1C=CC=CC=1.[F:7][C:8]1[CH:15]=[CH:14][C:11]([C:12]#[N:13])=[CH:10][C:9]=1[CH:16]([OH:18])[CH3:17]>C(Cl)Cl.CCOCC.[O-2].[O-2].[O-2].[Cr+6]>[C:12]([C:11]1[CH:14]=[CH:15][C:8]([F:7])=[C:9]([C:16](=[O:18])[CH3:17])[CH:10]=1)#[N:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 1049PyridineHCID 230001664-Fluoro-3-(1-hydroxyethyl)benzonitrile

生成物 1

HCID 230002093-Acetyl-4-fluorobenzonitrile

試薬・触媒・溶媒 3

HCID 10219390chromium (VI) trioxide触媒HCID 3283Diethyl Ether溶媒HCID 6344Dichloromethane溶媒2 回

実験手順

To a solution of pyridine (3.52 mL, 43.6 mmol) in CH2Cl2 (10 mL) was added dry chromium trioxide (2.18 g, 21.80 mmol) at 0° C. The reaction mixture was warmed to room temperature and stirred for 30 min. 4-fluoro-3-(1-hydroxyethyl)benzonitrile (600 mg, 3.63 mmol) dissolved in CH2Cl2 (10 mL) was added via canula. The reaction mixture was stirred for 10 min. and was diluted with ether and celite and stirred for an additional 20 min. The reaction mixture was filtered through a pad of celite and washed with ethyl acetate. The organic was washed then with 5% HCl and sat'd NaHCO3, brine, dried over MgSO4, and concentrated in vacuo to provide product:

後処理

  1. additionwas added via canula
  2. stirringThe reaction mixture was stirred for 10 min.
  3. stirringstirred for an additional 20 min
  4. filtrationThe reaction mixture was filtered through a pad of celite
  5. washwashed with ethyl acetate
  6. washThe organic was washed
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated in vacuo
  9. customto provide product

出典と根拠

ORDレコード
ord-038e7fabcbb3469f8fbe081927318655
出典データセット
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06610692B1

反応ノート

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