2-Amino-3-(methylthiomethyl)benzotrifluoride → 2-Amino-3-methylbenzotrifluoride
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
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
- stirringto stir overnight
- customMost but not all of the starting material had reacted
- customThe Raney nickel was removed by filtration
- washthe filter cake rinsed with 1200 ml of absolute ethanol
- concentrationthe filtrate concentrated
- dissolutionThe concentrate was dissolved in 100 ml of ethyl acetate
- washwashed with 70 ml of water
- dry with materialdried with magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customto yield 19.2 g of the crude product as a yellow oil which
- 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
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