Реакция #1183013

Уравнение реакции

1,4-dioxane

1,4-Dioxa-8-azaspiro[4,5]decane

1-(benzyloxy)-4-iodobenzene

sodium tert-butoxide

→

compound

Выход 73.6%

8-[4-(benzyloxy)phenyl]-1,4-dioxa-8-azaspiro[4,5]decane

Выход 73.6%

Растворители

ethyl acetate

Условия реакции

Обработка

1. 1
   ТемператураThe reaction solution was cooled with ice
2. 2
   Промывкаwashed with water and saturated saline in that order
3. 3
   Сушкаthe organic layer was dried with sodium sulfate
4. 4
   ДругоеThe solvent was evaporated off under reduced pressure
5. 5
   Другоеthe resulting residue was purified through silica gel column chromatography (eluate: chloroform/ethyl acetate=10/1)
6. 6
   Фильтрацияfiltered under suction

Методика

1,4-Dioxa-8-azaspiro[4,5]decane (653 g, 4.56 mol), 1-(benzyloxy)-4-iodobenzene (1 kg, 3.8 mol), sodium tert-butoxide (511 g, 5.32 mol), Pd(OAc)2 (17 g, 76 mmol) and biphenyl-2-yl(dicyclohexyl) phosphine (54 g, 152 mmol) were mixed, and 1,4-dioxane, this was stirred overnight at 80° C. in a nitrogen atmosphere. The reaction solution was cooled with ice, diluted with ethyl acetate, washed with water and saturated saline in that order, and the organic layer was dried with sodium sulfate. The solvent was evaporated off under reduced pressure, and the resulting residue was purified through silica gel column chromatography (eluate: chloroform/ethyl acetate=10/1), and the resulting crude product was suspended in a mixed solvent of chloroform/hexane and filtered under suction to obtain the entitled compound (910 g, 73%) as a brown solid.

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