Реакция #1533752

Уравнение реакции

Triethylamine

hydroxylamine hydrochloride

2,6-difluoroacetophenone

→

1-(2,6-difluorophenyl)ethylamine

Растворители

ethanol

Условия реакции

Обработка

1. 1
   Температураthe reaction solution was heated
2. 2
   Температураto reflux for 4 hours
3. 3
   Другоеwas returned to room temperature
4. 4
   Другоеthe solvent was evaporated under reduced pressure
5. 5
   workup.ADDITIONZinc (1.86 g) was added to a solution of the resulting residue in trifluoroacetic acid (10 mL)
6. 6
   ФильтрацияThe reaction solution was filtered on a celite
7. 7
   Экстракцияextracted with chloroform
8. 8
   СушкаThe resulting organic layer was dried over magnesium sulfate
9. 9
   Другоеthe solvent was evaporated under reduced pressure
10. 10
    Другоеto obtain 210 mg of a crude
11. 11
    Другоеpurified product
12. 12
    workup.ADDITIONcontaining the title compound (purity: 50 wt %)

Методика

Triethylamine (2.37 mL) and hydroxylamine hydrochloride (634 mg) were added to a solution of 2,6-difluoroacetophenone (890 mg) in ethanol (30 mL), and the reaction solution was heated to reflux for 4 hours. The reaction solution was returned to room temperature, and the solvent was evaporated under reduced pressure. Zinc (1.86 g) was added to a solution of the resulting residue in trifluoroacetic acid (10 mL), and the reaction solution was stirred at room temperature overnight. The reaction solution was filtered on a celite, made basic with a 5 N aqueous solution of sodium hydroxide, and then extracted with chloroform. The resulting organic layer was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure to obtain 210 mg of a crude purified product containing the title compound (purity: 50 wt %). The physical properties of the compound are as follows.

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