Dimethylformamide → 2-Bromo-3-chloro-6-fluorobenzaldehyde

HRID 2423078ノート

反応式

HRID 2423078 の反応式
C(NC(C)C)(C)C.C([Li])CCC.[Br:13][C:14]1[CH:19]=[C:18]([F:20])[CH:17]=[CH:16][C:15]=1[Cl:21].CN([CH:25]=[O:26])C>C1COCC1.O>[Br:13][C:14]1[C:15]([Cl:21])=[CH:16][CH:17]=[C:18]([F:20])[C:19]=1[CH:25]=[O:26]

参加物

7

反応条件

温度
-75 °C

実験手順

To a solution of diisopropylamine (5 mL, 35.4 mmol) in THF (30 mL) at 0° C. under argon was added n-butyl lithium (16.5 mL of 1.6 M solution in hexane, 26.4 mmol) slowly over 20 minutes. The mixture was cooled to −75° C. and 2-bromo-1-chloro-4-fluorobenzene (5 g, 23.9 mmol) in THF (20 mL) was added dropwise over 15 mins whilst maintaining the temperature <−70° C. The solution was then stirred at −75° C. for 45 mins and then DMF (2.2 mL, 28.6 mmol) was added over 5 mins. The mixture was stirred at −78° C. for 2 hrs and then allowed to reach room temperature. Water was added and the aqueous layer was extracted with ethyl acetate. The combined extracts were washed with brine and the solvent evaporated. Chromatography (silica gel, ethyl acetate/hexane) gave the title compound (D21) as a yellow solid (3.344 g)

後処理

  1. temperaturewhilst maintaining the temperature <−70° C
  2. stirringThe mixture was stirred at −78° C. for 2 hrs
  3. customto reach room temperature
  4. extractionthe aqueous layer was extracted with ethyl acetate
  5. washThe combined extracts were washed with brine
  6. customthe solvent evaporated

出典と根拠

ORDレコード
ord-7284bce253ed4c6c9d3e4ae04b4f575c
出典データセット
uspto-grants-2011_06
特許番号
US07960563B2

反応ノート

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