2-Amino-3-(methylthiomethyl)benzotrifluoride → 2-Amino-3-methylbenzotrifluoride

HRID 326991ノート

反応式

HRID 326991 の反応式
CS[CH2:3][C:4]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:14])([F:13])[F:12])[C:5]=1[NH2:6]>[Ni].C(O)C>[CH3:3][C:4]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:12])([F:13])[F:14])[C:5]=1[NH2:6]

参加物

4

実験手順

Several scoops of Raney nickel were added to 28.6 g of 2-{(methylthio)methyl}-6-(trifluoromethyl)aniline (Example 1A) in 50 ml of absolute ethanol. The reaction slurry was stirred at room temperature and the progress of the reaction was followed by gas-liquid chromatography (GLC). Periodically, additional Raney nickel was added to the reaction slurry. The reaction was allowed to stir overnight. Most but not all of the starting material had reacted. The Raney nickel was removed by filtration, the filter cake rinsed with 1200 ml of absolute ethanol and the filtrate concentrated. The concentrate was dissolved in 100 ml of ethyl acetate, washed with 70 ml of water, dried with magnesium sulfate, filtered, and concentrated to yield 19.2 g of the crude product as a yellow oil which was distilled at 30-40 torr, to give 6.2 g of the desired product at 93°-108° C. in 80% purity.

後処理

  1. stirringto stir overnight
  2. customMost but not all of the starting material had reacted
  3. customThe Raney nickel was removed by filtration
  4. washthe filter cake rinsed with 1200 ml of absolute ethanol
  5. concentrationthe filtrate concentrated
  6. dissolutionThe concentrate was dissolved in 100 ml of ethyl acetate
  7. washwashed with 70 ml of water
  8. dry with materialdried with magnesium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customto yield 19.2 g of the crude product as a yellow oil which
  12. distillationwas distilled at 30-40 torr

出典と根拠

ORDレコード
ord-dd547f27e5df4a0cbe83a7145f15d399
出典データセット
uspto-grants-1993_12
特許番号
US05272128

反応ノート

読み込み中…