Реакция #44007

Уравнение реакции

NH4Cl

Boron trifluoride dimethyl etherate

NH4OH

compound 66

benzyl 4-oxo-3,4-dihydropyridine-1(2H)-carboxylate

4-Chlorophenylmagnesium bromide

→

product 67

benzyl 2-(4-chlorophenyl)-4-oxopiperidine-1-carboxylate

Растворители

THF

THF

EtOAc

Условия реакции

Обработка

1. 1
   Другоеproduced an orange then green-like suspension
2. 2
   workup.STIRRINGstirred for 5 minutes
3. 3
   workup.STIRRINGAfter stirring 2 hours at −78° C.
4. 4
   Температураto warm-up to room temperature
5. 5
   Экстракцияto extract (3×100 mL)
6. 6
   Промывкаthe combined organic layers were washed with brine
7. 7
   Сушкаdried (MgSO4)
8. 8
   ДругоеSolvent was removed by rotary evaporation
9. 9
   Другоеthe residue was purified by flash chromatography

Методика

CuBr.SMe2 complex (1.49 g, 7.26 mmol) was added to 25 mL of anhydrous THF and cooled to −78° C. 4-Chlorophenylmagnesium bromide (7.26 mL, 1.0 M in THF, 7.26 mmol) was added slowly via syringe. Stirring at −78° C. for 1 hour produced an orange then green-like suspension. Boron trifluoride dimethyl etherate (0.92 mL, 7.26 mmol) was added and stirred for 5 minutes. To the newly formed complex was then added over 1 hour a solution of the compound 66 (1.0 g, 4.32 mmol) in 15 mL of anhydrous THF. After stirring 2 hours at −78° C., 16 mL of aq. 20% NH4Cl/conc. NH4OH (1:1) was added, and the mixture was allowed to warm-up to room temperature. EtOAc was used to extract (3×100 mL) and the combined organic layers were washed with brine and dried (MgSO4). Solvent was removed by rotary evaporation and the residue was purified by flash chromatography to give the product 67 as a colorless oil.

Источник