Hydrogen Peroxide → 3,5-Difluoro-4-difluoromethoxyphenol
反応式
FC1C=CC=C(F)C=1O.CCN(S(F)(F)F)CC.[F:19][C:20]1[CH:21]=[C:22]([OH:31])[CH:23]=[C:24]([F:30])[C:25]=1[O:26][CH:27]([F:29])[F:28].Br[C:33]1[CH:38]=[C:37]([F:39])[C:36]([O:40][CH:41]([F:43])[F:42])=[C:35]([F:44])[CH:34]=1.C(OO)(C)(C)C.OO>>[F:19][C:20]1[CH:21]=[C:22]([OH:31])[CH:23]=[C:24]([F:30])[C:25]=1[O:26][CH:27]([F:29])[F:28].[F:39][C:37]1[CH:38]=[CH:33][CH:34]=[C:35]([F:44])[C:36]=1[O:40][CH:41]([F:42])[F:43]参加物
反応物 6
生成物 2
実験手順
Compound (251) can be prepared in the same manner as in Preparation Example 248, except for replacing 3-fluoro-4-difluoromethoxyphenol with 3,5-difluoro-4-difluoromethoxyphenol. The 3,5-difluoro-4-difluoromethoxyphenol can be obtained by converting 2,6-difluorophenol to a formic ester, fluorinating the ester with DAST, brominating the resulting 2,6-difluoro-1-difluoromethoxybenzene, preparing a Grignard reagent from the resulting 4-bromo-2,6-difluoro-1-difluoromethoxybenzene, and reacting the Grignard reagent with t-butyl hydroperoxide or converting the Grignard reagent to a boric ester, and oxidizing the ester with hydrogen peroxide under a basic condition. Alternatively, 3,5-difluoro-4-difluoromethoxyphenol can also be obtained by nitrating 3,5-difluoro-4-difluoromethoxybenzene, reducing the product to 3-fluoro-4-trifluoromethoxyaniline, and decomposing a diazonium salt of the 3-fluoro-4-trifluoromethoxyaniline in sulfuric acid.
出典と根拠
- ORDレコード
- ord-2c735e53806d4ad984eb77fa9d50e4af
- 出典データセット
- uspto-grants-1996_07
- 特許番号
- US05536443
反応ノート
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