Tert-butyl 4-(1-ethoxy-1-oxopropan-2-yl)piperidine-1-carboxylate → Ethyl 2-(piperidin-4-yl)propanoate

HRID 1804840노트

반응식

HRID 1804840 반응식
[CH2:1]([O:3][C:4](=[O:20])[CH:5]([CH:7]1[CH2:12][CH2:11][N:10](C(OC(C)(C)C)=O)[CH2:9][CH2:8]1)[CH3:6])[CH3:2].Cl.O1CCOCC1>>[NH:10]1[CH2:11][CH2:12][CH:7]([CH:5]([CH3:6])[C:4]([O:3][CH2:1][CH3:2])=[O:20])[CH2:8][CH2:9]1

참가 물질

3

실험 절차

A sample of tert-butyl 4-(1-ethoxy-1-oxopropan-2-yl)piperidine-1-carboxylate (1.4 g, 4.91 mmol) was dissolved in 4 M hydrogen chloride/dioxane (5 mL, 165 mmol) and stirred at RT for 2 h. At the conclusion of this period, the mixture was concentrated on a rotary evaporator and the resultant residue was treated with saturated NaHCO3 and then 1 M NaOH to bring the pH to 9. The mixture was extracted with EtOAc. The extract was washed with brine, dried (MgSO4) and concentrated to give ethyl 2-(piperidin-4-yl)propanoate (0.85 g, 93%). 1H-NMR (400 MHz, CDCl3) δ ppm 4.05-4.13 (2 H, m), 2.99-3.08 (2 H, m), 2.54 (2 H, td, J=12.09, 2.52 Hz), 2.16-2.25 (1 H, m), 1.75 (1 H, s), 1.57-1.66 (2 H, m), 1.52 (1 H, dt, J=12.90, 2.86 Hz), 1.09-1.22 (1 H, m), 1.21 (3 H, t, J=7.18 Hz), 1.07 (3 H, d, J=7.05 Hz).

후처리

  1. concentrationAt the conclusion of this period, the mixture was concentrated on a rotary evaporator
  2. additionthe resultant residue was treated with saturated NaHCO3
  3. extractionThe mixture was extracted with EtOAc
  4. washThe extract was washed with brine
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-0a5099200e21456cb2da8600bf1169cd
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08354432B2

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