Ammonium Chloride → HCID 86602516、化合物

HRID 30704

反応式

HRID 30704 の反応式
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

7

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

  1. temperatureto warm from −78° C. to room temperature
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe organic layer was washed successively with 1N hydrochloric acid, water and saturated brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. 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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