反応式
C(N1CCC(CN[C:12]([NH:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2F)=[S:13])CC1)(=O)C.[F:22][C:23]1[CH:28]=[CH:27][C:26]([C:29](=[O:31])[CH3:30])=[C:25]([OH:32])[CH:24]=1.Cl[CH2:34][C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1.C(=O)([O-])[O-:42].[K+].[K+].[I-].[K+]>CC(=O)C>[N:14]([C:15]1[CH:16]=[CH:17][C:18]2[O:42][CH2:30][CH2:29][O:31][C:19]=2[CH:20]=1)=[C:12]=[S:13].[F:22][C:23]1[CH:28]=[CH:27][C:26]([C:29](=[O:31])[CH3:30])=[C:25]([O:32][CH2:34][C:35]2[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=2)[CH:24]=1参加物
8
反応物 5
生成物 2
試薬・触媒・溶媒 1
実験手順
A mixture of 13 parts of 1-(4-fluoro-2-hydroxyphenyl)ethanone, 14.9 parts of (chloromethyl)benzene, 16.4 parts of potassium carbonate, 0.1 parts of potassium iodide and 120 parts of 2-propanone was stirred overnight at reflux temperature. The reaction mixture was evaporated. The reaction mixture was poured into water. The product was extracted three times with trichloromethane. The combined extracts were dried, filtered and evaporated. The residue was crystallized from a mixture of 2-propanol and water. The product was filtered off and dried, yielding 11 parts (58%) of 1-[4-fluoro-2-(phenylmethoxy)phenyl]ethanone (intermediate 76).
後処理
- temperatureat reflux temperature
- customThe reaction mixture was evaporated
- additionThe reaction mixture was poured into water
- extractionThe product was extracted three times with trichloromethane
- customThe combined extracts were dried
- filtrationfiltered
- customevaporated
- customThe residue was crystallized from a mixture of 2-propanol and water
- filtrationThe product was filtered off
- customdried
出典と根拠
- ORDレコード
- ord-999acce87e7e48318b5901a2eb848d87
- 出典データセット
- uspto-grants-1988_06
- 特許番号
- US04749702
関連ノート
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