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

HRID 1533835
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HRID 1533835 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6228Dimethylformamide2회HCID 5231012-Fluoro-6-methoxybenzonitrileHCID 129663835Sodium triazolide

생성물 1

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

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온도
0 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-64c7b8a49f8549c799be7c03c0040576
출처 데이터셋
uspto-grants-1992_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05085686

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