Hydrochloric Acid → HCID 22618361、化合物
反応式
[CH3:1][Mg]I.[Cl:4][C:5]1[CH:10]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:8]=[C:7]([Cl:15])[C:6]=1[N:16]1[CH:20]=C(C#N)[C:18]([C:23]([F:26])([F:25])[F:24])=[N:17]1.Cl.C([O:30][CH2:31][CH3:32])C>>[C:31]([C:32]1[C:18]([C:23]([F:26])([F:24])[F:25])=[N:17][N:16]([C:6]2[C:7]([Cl:15])=[CH:8][C:9]([C:11]([F:13])([F:14])[F:12])=[CH:10][C:5]=2[Cl:4])[CH:20]=1)(=[O:30])[CH3:1]参加物
実験手順
A solution of methylmagnesium iodide (prepared from magnesium (0.26 g) and methyl iodide (1.5 g) in diethyl ether (25 ml)), was treated with a solution of 1-(2,6-dichloro-4-trifluoromethylphenyl)-4-cyano-3-trifluoromethylpyrazole (2 g) in diethyl ether (20 ml), dropwise. The resulting pale yellow solution was refluxed for 24 hours, cooled, and treated with hydrochloric acid (2N, 10 ml). After stirring for 0.5 hour at room temperature, the reaction mixture was diluted with ether (50 ml). The ethereal extract was washed with water (50 ml), dried over anhydrous magnesium sulphate, and evaporated in vacuo to give a yellow gum. This was purified by chromatography on silica (Merck, 200-400 mesh, 0.7 kg cm-2) eluting with a mixture of dichloromethane and petroleum ether (4:1) to give 4-acetyl-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-trifluoromethylpyrazole as a white solid, m.p. 134° C.
後処理
- temperatureThe resulting pale yellow solution was refluxed for 24 hours
- temperaturecooled
- extractionThe ethereal extract
- washwas washed with water (50 ml)
- dry with materialdried over anhydrous magnesium sulphate
- customevaporated in vacuo
- customto give a yellow gum
- customThis was purified by chromatography on silica (Merck, 200-400 mesh, 0.7 kg cm-2)
- washeluting with a mixture of dichloromethane and petroleum ether (4:1)
出典と根拠
- ORDレコード
- ord-0a7a2cdadaa64e9c89f904a2446ef8cd
- 出典データセット
- uspto-grants-1998_02
- 特許番号
- US05714191
反応ノート
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