Trichloroacetyl chloride → HCID 70922409、化合物

HRID 524974ノート

反応式

HRID 524974 の反応式
[Cl:1][C:2]([Cl:7])([Cl:6])[C:3](Cl)=[O:4].[CH3:8][C:9]1[CH:13]=[CH:12][NH:11][CH:10]=1>C(OCC)C>[Cl:1][C:2]([Cl:7])([Cl:6])[C:3]([C:12]1[NH:11][CH:10]=[C:9]([CH3:8])[CH:13]=1)=[O:4]

参加物

4

反応条件

温度
45 °C

実験手順

To a solution of 2,2,2-trichloroacetyl chloride (5.05 mL, 45.3 mmol) in dry diethyl ether (12 mL) was slowly added a solution of 3-methyl-1H-pyrrole (3.15 g, 39.37 mmol) in 30 mL of dry diethyl ether during 1 h 15 min. Once the addition was finished, the reaction mixture was stirred at 45° C. during 1 hour 30 minutes more. Next, more diethyl ether was added and the organic phase was washed with an aqueous solution of potassium carbonate to neutralize de media, water and brine. The organic phase was dried (Na2SO4) and concentrated to dryness to give a residue that was purified by flash chromatography silica (hexane/dichloromethane) to afford 4.7 g of the title compound (55% yield).

後処理

  1. additionOnce the addition
  2. washthe organic phase was washed with an aqueous solution of potassium carbonate
  3. dry with materialThe organic phase was dried (Na2SO4)
  4. concentrationconcentrated to dryness
  5. customto give a residue that
  6. customwas purified by flash chromatography silica (hexane/dichloromethane)

出典と根拠

ORDレコード
ord-d8226630e89d4b779ad86ddefaff351f
出典データセット
uspto-grants-2016_05
特許番号
US09340547B2

反応ノート

読み込み中…