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Pyrrolidine → 1-(4-nitrophenethyl)pyrrolidine

HRID 2236444
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HRID 2236444 반응식
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.Br[CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][C:12]([N+:15]([O-:17])=[O:16])=[CH:11][CH:10]=1.C([O-])(O)=O.[Na+]>CC#N>[N+:15]([C:12]1[CH:13]=[CH:14][C:9]([CH2:8][CH2:7][N:1]2[CH2:5][CH2:4][CH2:3][CH2:2]2)=[CH:10][CH:11]=1)([O-:17])=[O:16]
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참가 물질

5

반응물 3

HCID 31268PyrrolidineHCID 792664-Nitrophenethyl bromideHCID 516892Sodium Bicarbonate

생성물 1

HCID 105369011-(4-nitrophenethyl)pyrrolidine

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
0 °C

실험 절차

Pyrrolidine (3.89 g, 54.8 mmol) is added to a mixture of 8.40 g (36.5 mmol) of 1-(2-bromoethyl)-4-nitrobenzene and 6.14 g (73.0 mmol) of NaHCO3 in 60 mL of CH3CN at 0° C. The mixture is stirred for 0.5 h at 0° C. and then at 25° C. overnight. The reaction is filtered, the insoluble material is washed with CH3CN and the filtrate and wash were combined. Darco is added, the solution is dried (MgSO4) and evaporated to a viscous red oil. Stirring this material with Et2O caused crystallization of the product. It is collected, washed with Et2O and dried in vacuo to give 7.60 g (95%) of a tan hygroscopic solid. 1H NMR (DMSO-d6) δ 8.22 (d, 2H, J=6.57 Hz), 7.62 (d, 2H, J=6.57 Hz), 3.47 (m, 2H), 3.25 (m, 2H), 3.10 (m, 4H), 1.94 (m, 4H); MS (ESI) m/z 221.2 (M+1).

후처리

  1. customat 25° C.
  2. customovernight
  3. filtrationThe reaction is filtered
  4. washthe insoluble material is washed with CH3CN
  5. washthe filtrate and wash
  6. additionDarco is added
  7. dry with materialthe solution is dried (MgSO4)
  8. customevaporated to a viscous red oil
  9. stirringStirring this material with Et2O
  10. customcrystallization of the product
  11. customIt is collected
  12. washwashed with Et2O
  13. customdried in vacuo
  14. customto give 7.60 g (95%) of a tan hygroscopic solid

출처 및 근거

ORD 기록
ord-1525c9ededdb4cef9cf22e2b59a88435
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07713994B2

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