تفاعل #685024
ord-f009d28e78c04276a7da1ea5be3ef8c9
معادلة التفاعل
الكواشف
ظروف التفاعل
المعالجة
- 1أخرىAfter quenching with water
- 2workup.ADDITIONthe organic phase was diluted with EtOAc
- 3غسيلwashed with water, brine
- 4تجفيفdried (Na2SO4)
- 5تركيزAfter concentration
- 6أخرىthe residue was purified by flash chromatography (10% to 20% EtOAc/hexane)
الإجراء التجريبي
To a stirred solution of benzyl 4-cyanopiperidine-1-carboxylate (10 g, 41 mmol) and iodo-tert-butyldimethylsilane butane (12.6 mL, 49 mmol) in THF (80 mL) cooled to −78° C. was added LiHMDS (50 mL, 50 mmol, 1M in THF) dropwise over 30 min. The resulting mixture was stirred while gradually warming to room temperature for 18 h. After quenching with water, the organic phase was diluted with EtOAc and washed with water, brine and dried (Na2SO4). After concentration, the residue was purified by flash chromatography (10% to 20% EtOAc/hexane) to give the title compound as yellow oil (11.88 g, 67% yield). 1H NMR (300 MHz, CDCl3) δ: 7.34-7.28 (5H, m), 5.09 (2H, s), 4.17 (2H, bs), 3.59 (2H, t, J=5.3 Hz), 3.07 (2H, bs), 1.89 (2H, d, J=13.2 Hz), 1.53 (6H, bs), 1.43-1.34 (2H, m), 0.85 (9H, s), 0.01 (6H, s). LCMS (M+H): 431.20.