反応式
ClC1C=CC=C(Cl)C=1C=O.FC1C=CC=C(Cl)C=1C=O.FC1C=CC=C(Cl)C=1CO.[F:31][C:32]1[CH:39]=[CH:38][CH:37]=[C:36]([F:40])[C:33]=1[CH:34]=[O:35]>>[F:31][C:32]1[CH:39]=[CH:38][CH:37]=[C:36]([F:40])[C:33]=1[CH2:34][OH:35]参加物
5
実験手順
Particularly preferably, 2,6-dichlorobenzaldehyde is used in the process of the invention and 2-fluoro-6-chlorobenzaldehyde, 2-fluoro-6-chlorobenzyl alcohol, 2,6-difluorobenzaldehyde or 2,6-difluorobenzyl alcohol is obtained or 2,4-dichlorobenzaldehyde is used and 2,4-difluoro-benzaldehyde or 2,4-difluorobenzyl alcohol is obtained or 3,4-dichloro-benzaldehyde is used and 3-chloro-4-fluorobenzaldehyde or 3-chloro-4-fluorobenzyl alcohol is obtained.
出典と根拠
- ORDレコード
- ord-5ca6a953926b46579b64bfd1dcfe0c95
- 出典データセット
- uspto-grants-2000_10
- 特許番号
- US06127581
関連ノート
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