Реакция #586139

Уравнение реакции

[5-(2,6-dichloro-4-trifluoromethylphenyl)-2-nitrophenyl] isopropyl sulfide

compound

methyl 2-propylthio-4-(3-trifluoromethylpyrazolyl)benzoate

water

acetic acid

→

4-(2,6-dichloro-4-trifluoromethylphenyl)-2-isopropylthioaniline

Выход 36.0%

Растворители

toluene

toluene

Условия реакции

Обработка

1. 1
   Температураwith reflux
2. 2
   Температураheating for another 3 hours
3. 3
   ФильтрацияThe insolubles were filtered off
4. 4
   Другоеthe filtrate was separated with water and toluene
5. 5
   ПромывкаThe toluene layer was washed with water
6. 6
   Сушкаdried over anhydrous magnesium sulfate
7. 7
   workup.DISTILLATIONthe solvent was distilled off under reduced pressure
8. 8
   ДругоеPurification of the residue by silica gel column chromatography

Методика

3.5 g (63.6 mmol) of iron powder, 10 m of water and 1 m of acetic acid were stirred in 20 ml toluene at 60° C. for 30 minutes, and 3.0 g (7.3 mmol) of [5-(2,6-dichloro-4-trifluoromethylphenyl)-2-nitrophenyl] isopropyl sulfide (the compound prepared in Example 8 (2)) in 10 ml toluene was added dropwise. The reaction was carried out with reflux and heating for another 3 hours, and then the reaction mixture was cooled to room temperature. The insolubles were filtered off, and the filtrate was separated with water and toluene. The toluene layer was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 1.0 g of 4-(2,6-dichloro-4-trifluoromethylphenyl)-2-isopropylthioaniline (yield 36.0%) as a pale yellow dough (nD20 1.5782).

Источник