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Dimethylformamide → 2-Methoxy-6-(1,2,4-triazol-1-yl)-benzonitrile

HRID 1533835
ノート
印刷プレビュー

反応式

HRID 1533835 の反応式
[CH3:1][O:2][C:3]1[CH:10]=[CH:9][CH:8]=[C:7](F)[C:4]=1[C:5]#[N:6].N1C=[C-:15][N:14]=[N:13]1.[Na+].[CH3:18][N:19](C)C=O>>[CH3:1][O:2][C:3]1[CH:10]=[CH:9][CH:8]=[C:7]([N:14]2[CH:15]=[N:19][CH:18]=[N:13]2)[C:4]=1[C:5]#[N:6]
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

4

反応物 3

HCID 6228Dimethylformamide2 回HCID 5231012-Fluoro-6-methoxybenzonitrileHCID 129663835Sodium triazolide

生成物 1

HCID 197799332-Methoxy-6-(1,2,4-triazol-1-yl)-benzonitrile

反応条件

温度
0 °C

実験手順

A solution of 30.2 g (0.20 mol) of 2-methoxy-6-fluorobenzonitrile [preparation: J. Heterocycl. Chem. 25 (1988), 1173]in 50 ml of N,N-dimethylformamide is added dropwise at 45°-50° C., under nitrogen, to a solution of 0.21 mol of sodium triazolide (prepared from equimolar amounts of triazol and sodium hydride) in 100 ml of N,N-dimethylformamide, and the mixture is stirred for 2 h at 0° C. After the solvent has been evaporated under reduced pressure, the residue is stirred with 200 ml of ice water, the pH is brought to 6 with a little glacial acetic acid and the solid is filtered off under suction and dried. After the addition of a little ether, 35 g of the product of melting point 169°-171° C. (decomposition) are obtained.

後処理

  1. customAfter the solvent has been evaporated under reduced pressure
  2. stirringthe residue is stirred with 200 ml of ice water
  3. filtrationthe solid is filtered off under suction
  4. customdried
  5. additionAfter the addition of a little ether, 35 g of the product of melting point 169°-171° C. (decomposition)
  6. customare obtained

出典と根拠

ORDレコード
ord-64c7b8a49f8549c799be7c03c0040576
出典データセット
uspto-grants-1992_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05085686

反応ノート

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