Phenylacetonitrile → 1-Tert-butyl-4-phenylpiperidine-4-carbonitrile

HRID 1800821

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HRID 1800821 반응식
[C:1]1([CH2:7][C:8]#[N:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[Na+].Cl[CH2:13][CH2:14][N:15]([CH2:20][CH2:21]Cl)[C:16]([CH3:19])([CH3:18])[CH3:17]>CS(C)=O.Cl>[C:16]([N:15]1[CH2:20][CH2:21][C:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)([C:8]#[N:9])[CH2:13][CH2:14]1)([CH3:19])([CH3:18])[CH3:17]

참가 물질

6

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온도
23 °C

실험 절차

A solution of phenyl acetonitrile (1.0 g, 8.54 mmol) in DMSO (8 mL) was treated with sodium hydride (0.717 g, 29.88 mmol) portionwise. The resulting-suspension was stirred at 23° C. for 30 minutes. N,N-bis(2-chloroethyl)-2-methylpropan-2-amine (2.20 g, 9.39 mmol) was then slowly added over 5 minutes, then the suspension was heated at 65° C. overnight. The reaction was then diluted with 1N hydrochloric acid and washed with ethyl acetate (2×). The aqueous phase was basified with sat. aq. sodium carbonate and extracted with ethyl acetate (3×). The combined extracts were washed with water (5×), dried over anhydrous magnesium sulfate, filtered and concentrated to give an oil (1.40 g, 68%) which solidified on standing and was used as such for the next reaction. 1H NMR (400 MHz, CDCl3) δ ppm: 2.10-2.17 (3H, m), 2.31-2.37 (1H, m), 2.42 (3H, s), 2.47-2.57 (2H, m), 3.01 (2G, d, J=12.6 Hz), 7.45 (2H, dd, J=4.55 and 1.52 Hz), 8.68 (2H, dd, J=4.55 and 1.77 Hz).

후처리

  1. temperaturethe suspension was heated at 65° C. overnight
  2. washwashed with ethyl acetate (2×)
  3. extractionextracted with ethyl acetate (3×)
  4. washThe combined extracts were washed with water (5×)
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-fbd69499da744215af03b08e7a414372
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08343999B2

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