Pyridine → (1-methyl-1H-tetrazol-5-yl)(phenyl)methanone

HRID 42717

反応式

HRID 42717 の反応式
[C:1](Cl)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:10][N+:11]#[C-:12].[N-:13]=[N+:14]=[N-:15].[Na+].N1C=CC=CC=1>C(#N)C.C(OCC)(=O)C.O>[CH3:12][N:11]1[C:10]([C:1](=[O:8])[C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[N:15][N:14]=[N:13]1

参加物

8

反応条件

温度
60 °C

実験手順

At room temperature, 10 g of benzoyl chloride (71 mmol) were admixed with 3.7 g (92 mmol) of methyl isocyanide. The mixture was then heated at 60° C. for 3 hours. The mixture was admixed with 25 ml of acetonitrile and cooled to 0° C. This reaction mixture was added to 4.6 g of sodium azide (71 mmol) in 1.1 g (14 mmol) of pyridine in 25 ml of acetonitrile at 0° C. The mixture was then heated to 60° C. and stirred at this temperature for 1 hour. At room temperature, 100 ml of water and 100 ml of ethyl acetate were added to the mixture. The organic phase was separated off and the aqueous phase was extracted with 100 ml of ethyl acetate. The combined organic phases were dried over magnesium sulphate and the solvent was removed in vacuo. The crude product was recrystallized from 20 ml of isopropanol, giving 8.83 g of 1-methyl-5-benzoyltetrazole (purity 99.6%).

後処理

  1. customAt room temperature
  2. temperaturecooled to 0° C
  3. temperatureThe mixture was then heated to 60° C.
  4. customThe organic phase was separated off
  5. extractionthe aqueous phase was extracted with 100 ml of ethyl acetate
  6. dry with materialThe combined organic phases were dried over magnesium sulphate
  7. customthe solvent was removed in vacuo
  8. customThe crude product was recrystallized from 20 ml of isopropanol

出典と根拠

ORDレコード
ord-e367809a15df44d488c35606de51a174
出典データセット
uspto-grants-2013_09
特許番号
US08536211B2

関連ノート

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