Trifluoromethanesulfonic anhydride → 4-Cyano-2-methoxyphenyl trifluoromethanesulfonate

HRID 1947236ノート

反応式

HRID 1947236 の反応式
[F:1][C:2]([F:15])([F:14])[S:3]([O:6]S(C(F)(F)F)(=O)=O)(=[O:5])=[O:4].O[C:17]1[CH:24]=[CH:23][C:20]([C:21]#[N:22])=[CH:19][C:18]=1[O:25][CH3:26]>N1C=CC=CC=1>[F:1][C:2]([F:15])([F:14])[S:3]([O:6][C:17]1[CH:24]=[CH:23][C:20]([C:21]#[N:22])=[CH:19][C:18]=1[O:25][CH3:26])(=[O:5])=[O:4]

参加物

4

反応物 2

HCID 67749Trifluoromethanesulfonic anhydrideHCID 781354-Hydroxy-3-methoxybenzonitrile

生成物 1

HCID 166592584-Cyano-2-methoxyphenyl trifluoromethanesulfonate

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

24 ml (141 mmol) of trifluoromethanesulfonic anhydride are slowly added dropwise to a solution of 20 g (134 mmol) of 4-hydroxy-3-methoxybenzonitrile in pyridine (80 ml), keeping the reaction temperature below 25° C. with the aid of an ice bath. The suspension is then stirred at RT for 1 h. Ice-water (400 ml) is added, and the suspension is stirred further until room temperature is reached. It is then filtered, the solid is dissolved in ethyl acetate, and this solution is washed with saturated sodium chloride solution. The organic phase is dried over magnesium sulfate and concentrated. 37.13 g (92% of theory) of the title compound are obtained as a white solid.

後処理

  1. customthe reaction temperature below 25° C.
  2. stirringthe suspension is stirred further until room temperature
  3. filtrationIt is then filtered
  4. dissolutionthe solid is dissolved in ethyl acetate
  5. washthis solution is washed with saturated sodium chloride solution
  6. dry with materialThe organic phase is dried over magnesium sulfate
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-747b86e4fc784569b72ce5b26dbf25a2
出典データセット
uspto-grants-2013_03
特許番号
US08399471B2

反応ノート

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