Реакция #1759556

Уравнение реакции

1-tert-Butyl 2-methyl (2S)-pyrrolidine-1,2-dicarboxylate

lithium hexamethyldisilazide

1-bromo-3-methylbut-2-ene

→

desired product

1-tert-Butyl 2-methyl 2-(3-methylbut-2-en-1-yl)pyrrolidine-1,2-dicarboxylate

Растворители

THF

THF

Условия реакции

Обработка

1. 1
   ДругоеThe reaction was quenched by the drop-wise addition of saturated NH4Cl (15 mL)
2. 2
   ТемператураAfter gradually warming to room temperature (RT)
3. 3
   workup.ADDITIONthe reaction mixture was diluted with EtOAc (100 mL) and water (10 mL)
4. 4
   ПромывкаThe organic layer was washed with water (15 mL)
5. 5
   Экстракцияthe combined aqueous phases were extracted with EtOAc several times
6. 6
   ПромывкаThe combined organic phases were washed with brine
7. 7
   Сушкаdried (Na2SO4)
8. 8
   Концентрированиеconcentrated in vacuo

Методика

1-tert-Butyl 2-methyl (2S)-pyrrolidine-1,2-dicarboxylate (2.29 g, 0.00999 mol) was dissolved in anhydrous THF (30 mL) and the solution was cooled to −78° C. prior to the drop-wise addition of 1.0 M of lithium hexamethyldisilazide in THF (16 mL) over 15 min. After stirring for 1 h, 1-bromo-3-methylbut-2-ene (1.6 mL, 0.014 mol) was added and the resultant solution was stirred for 5 hours at −78° C. The reaction was quenched by the drop-wise addition of saturated NH4Cl (15 mL). After gradually warming to room temperature (RT), the reaction mixture was diluted with EtOAc (100 mL) and water (10 mL). The organic layer was washed with water (15 mL) and the combined aqueous phases were extracted with EtOAc several times. The combined organic phases were washed with brine, dried (Na2SO4), and concentrated in vacuo to afford the desired product, which was used in the subsequent step without further purification. LC-MS: 198.2 (M−Boc+2H)+ and 320.2 (M+Na)+.

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