反応式
C[Si]([N-][Si](C)(C)C)(C)C.[K+].[CH3:11][O:12][C:13]([CH2:15]P(=O)(OCC(F)(F)F)OCC(F)(F)F)=[O:14].C1OCCOCCOCCOCCOCCOC1.[F:48][C:49]1[CH:54]=[CH:53][C:52]([C:55]2[N:59]([CH3:60])[N:58]=[CH:57][C:56]=2[CH:61]=O)=[CH:51][CH:50]=1.[Cl-].[NH4+]>O1CCCC1>[F:48][C:49]1[CH:50]=[CH:51][C:52]([C:55]2[N:59]([CH3:60])[N:58]=[CH:57][C:56]=2/[CH:61]=[CH:15]\[C:13]([O:12][CH3:11])=[O:14])=[CH:53][CH:54]=1参加物
実験手順
Potassium bis(trimethylsilyl)amide (20% toluene solution, 3.05 g) was added to a mixture of bis(2,2,2-trifluoroethyl) (methoxycarbonylmethyl)phosphonate (973 mg), 18-crown-6 (4.04 g) and tetrahydrofuran (50 mL) at −78° C. Furthermore, 5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehyde (312 mg) was added and the mixture was stirred overnight while allowing to warm from −78° C. to room temperature. Saturated aqueous ammonium chloride was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed successively with 1N hydrochloric acid, water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to give methyl (2Z)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylate as crystals (0.35 g, yield 95%) from a fraction eluted with hexane-ethyl acetate (4:1-1:1, v/v) (recrystallized from ethyl acetate-hexane). melting point: 108-109° C.
後処理
- temperatureto warm from −78° C. to room temperature
- extractionthe mixture was extracted with ethyl acetate
- washThe organic layer was washed successively with 1N hydrochloric acid, water and saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-c8b7e21fd74f477c8b910c5ce184dcd9
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07423159B2
関連ノート
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