Imidazole → 2,4-Dichloro-beta-(1-imidazolyl)propiophenone
反応式
C(C(C1C=[CH:9][C:8]([Cl:11])=[CH:7]C=1Cl)=O)=C.[Cl:13][C:14]1[CH:19]=C(Cl)C=CC=1C(C=C)O.Br[C:26]1[C:27](=O)[C:28](Br)=[CH:29][C:30](Br)(Br)[CH:31]=1.[NH:36]1C=C[N:38]=[CH:37]1.CC[O:43]CC>>[Cl:11][CH:8]([CH2:7][N:36]1[CH:19]=[C:14]([Cl:13])[N:38]=[CH:37]1)[C:9]([C:26]1[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=1)=[O:43]参加物
6
実験手順
7.0 g. of 2,4-dichlorophenyl vinyl ketone (prepared by Jones oxidation of 2,4-dichlorophenyl vinyl carbinol using the general method described in J. Chem. Soc. (C), 1966, p. 1972) in 350 ml. of anhydrous ether was treated with 3.5 g. of imidazole, the solution stirred overnight and then washed with water (3 × 30 ml.). The solution is dried (MgSO4) and evaporated to give 2,4-dichloro-β-(1-imidazolyl)propiophenone as an amber gum (8.65 g.). The hydrochloride salt may be precipitated from ether and recrystallized from methanol/acetone as colorless rods, m.p. 105.5°-110° C.
後処理
- washwashed with water (3 × 30 ml.)
- dry with materialThe solution is dried (MgSO4)
- customevaporated
出典と根拠
- ORDレコード
- ord-2b1a10289aac4060948347073ffdb68f
- 出典データセット
- uspto-grants-1977_08
- 特許番号
- US04045568
反応ノート
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